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LitCoin-entities-OrganismTaxon-PD

Id Subject Object Predicate Lexical cue db_id
T1 254-259 OrganismTaxon denotes human NCBItxid:9606

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T1 0-139 Sentence denotes Single nucleotide polymorphisms of the HNF4alpha gene are associated with the conversion to type 2 diabetes mellitus: the STOP-NIDDM trial.
T2 140-288 Sentence denotes Hepatocyte nuclear factor 4alpha (HNF4alpha) is a transcription factor, which is necessary for normal function of human liver and pancreatic islets.
T3 289-510 Sentence denotes We investigated whether single nucleotide polymorphisms (SNPs) of HNF4A, encoding HNF4alpha, influenced the conversion from impaired glucose tolerance (IGT) to type 2 diabetes mellitus in subjects of the STOP-NIDDM trial.
T4 511-631 Sentence denotes This trial aimed at evaluating the effect of acarbose compared to placebo in the prevention of type 2 diabetes mellitus.
T5 632-789 Sentence denotes Eight SNPs covering the intragenic and alternate P2 promoter regions of HNF4A were genotyped in study samples using the TaqMan Allelic Discrimination Assays.
T6 790-987 Sentence denotes Three SNPs in the P2 promoter region (rs4810424, rs1884614, and rs2144908) were in almost complete association (D'>0.97, r (2)>0.95) and, therefore, only rs4810424 was included in further analyses.
T7 988-1316 Sentence denotes Female carriers of the less frequent C allele of rs4810424 had a 1.7-fold elevated risk [95% confidence interval (CI) 1.09-2.66; P=0.020] for the conversion to diabetes compared to women with the common genotype after the adjustment for age, treatment group (placebo or acarbose), smoking, weight at baseline, and weight change.
T8 1317-1349 Sentence denotes No association was found in men.
T9 1350-1633 Sentence denotes Haplotype analysis based on three SNPs (rs4810424, rs2071197, and rs3818247) representing the linkage disequilibrium blocks in our study population indicated that the conversion to type 2 diabetes mellitus was dependent on the number of risk alleles in different haplotypes in women.
T10 1634-1787 Sentence denotes Our results suggest that SNPs of HNF4A and their haplotypes predispose to type 2 diabetes mellitus in female subjects of the STOP-NIDDM study population.

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
3149 39-48 GeneOrGeneProduct denotes HNF4alpha NCBIGene:3172
3150 92-116 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus MESH:D003924
3151 140-172 GeneOrGeneProduct denotes Hepatocyte nuclear factor 4alpha NCBIGene:3172
3152 174-183 GeneOrGeneProduct denotes HNF4alpha NCBIGene:3172
3153 254-259 OrganismTaxon denotes human NCBITaxon:9606
3154 355-360 GeneOrGeneProduct denotes HNF4A NCBIGene:3172
3155 371-380 GeneOrGeneProduct denotes HNF4alpha NCBIGene:3172
3156 413-439 DiseaseOrPhenotypicFeature denotes impaired glucose tolerance MESH:D018149
3157 441-444 DiseaseOrPhenotypicFeature denotes IGT MESH:D018149
3158 449-473 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus MESH:D003924
3159 556-564 ChemicalEntity denotes acarbose MESH:D020909
3160 606-630 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus MESH:D003924
3161 704-709 GeneOrGeneProduct denotes HNF4A NCBIGene:3172
3162 828-837 SequenceVariant denotes rs4810424 DBSNP:rs4810424
3163 839-848 SequenceVariant denotes rs1884614 DBSNP:rs1884614
3164 854-863 SequenceVariant denotes rs2144908 DBSNP:rs2144908
3165 944-953 SequenceVariant denotes rs4810424 DBSNP:rs4810424
3166 1037-1046 SequenceVariant denotes rs4810424 DBSNP:rs4810424
3167 1148-1156 DiseaseOrPhenotypicFeature denotes diabetes MESH:D003920
3168 1169-1174 OrganismTaxon denotes women NCBITaxon:9606
3169 1258-1266 ChemicalEntity denotes acarbose MESH:D020909
3170 1345-1348 OrganismTaxon denotes men NCBITaxon:9606
3171 1390-1399 SequenceVariant denotes rs4810424 DBSNP:rs4810424
3172 1401-1410 SequenceVariant denotes rs2071197 DBSNP:rs2071197
3173 1416-1425 SequenceVariant denotes rs3818247 DBSNP:rs3818247
3174 1531-1555 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus MESH:D003924
3175 1627-1632 OrganismTaxon denotes women NCBITaxon:9606
3176 1667-1672 GeneOrGeneProduct denotes HNF4A NCBIGene:3172
3177 1708-1732 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus MESH:D003924

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 92-116 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus 0005148
T2 99-116 DiseaseOrPhenotypicFeature denotes diabetes mellitus 0005015
T3 270-280 DiseaseOrPhenotypicFeature denotes pancreatic 0004982
T4 449-473 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus 0005148
T5 456-473 DiseaseOrPhenotypicFeature denotes diabetes mellitus 0005015
T6 606-630 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus 0005148
T7 613-630 DiseaseOrPhenotypicFeature denotes diabetes mellitus 0005015
T8 880-888 DiseaseOrPhenotypicFeature denotes complete 0700063
T9 1531-1555 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus 0005148
T10 1538-1555 DiseaseOrPhenotypicFeature denotes diabetes mellitus 0005015
T11 1708-1732 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus 0005148
T12 1715-1732 DiseaseOrPhenotypicFeature denotes diabetes mellitus 0005015

LitCoin-SeqVar

Id Subject Object Predicate Lexical cue
T1 828-837 SequenceVariant denotes rs4810424
T2 839-848 SequenceVariant denotes rs1884614
T3 854-863 SequenceVariant denotes rs2144908
T4 944-953 SequenceVariant denotes rs4810424
T5 1037-1046 SequenceVariant denotes rs4810424
T6 1390-1399 SequenceVariant denotes rs4810424
T7 1401-1410 SequenceVariant denotes rs2071197
T8 1416-1425 SequenceVariant denotes rs3818247

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 39-48 GeneOrGeneProduct denotes HNF4alpha
T2 92-98 GeneOrGeneProduct denotes type 2
T3 99-107 GeneOrGeneProduct denotes diabetes
T4 122-126 GeneOrGeneProduct denotes STOP
T5 159-165 GeneOrGeneProduct denotes factor
T6 166-172 GeneOrGeneProduct denotes 4alpha
T7 174-183 GeneOrGeneProduct denotes HNF4alpha
T8 190-210 GeneOrGeneProduct denotes transcription factor
T9 260-265 GeneOrGeneProduct denotes liver
T10 281-287 GeneOrGeneProduct denotes islets
T11 355-360 GeneOrGeneProduct denotes HNF4A
T12 371-380 GeneOrGeneProduct denotes HNF4alpha
T13 430-439 GeneOrGeneProduct denotes tolerance
T14 449-455 GeneOrGeneProduct denotes type 2
T15 456-464 GeneOrGeneProduct denotes diabetes
T16 493-497 GeneOrGeneProduct denotes STOP
T17 606-612 GeneOrGeneProduct denotes type 2
T18 613-621 GeneOrGeneProduct denotes diabetes
T19 704-709 GeneOrGeneProduct denotes HNF4A
T20 873-879 GeneOrGeneProduct denotes almost
T21 995-1003 GeneOrGeneProduct denotes carriers
T22 1047-1052 GeneOrGeneProduct denotes had a
T23 1057-1061 GeneOrGeneProduct denotes fold
T24 1148-1156 GeneOrGeneProduct denotes diabetes
T25 1369-1374 GeneOrGeneProduct denotes based
T26 1467-1473 GeneOrGeneProduct denotes blocks
T27 1531-1537 GeneOrGeneProduct denotes type 2
T28 1538-1546 GeneOrGeneProduct denotes diabetes
T29 1667-1672 GeneOrGeneProduct denotes HNF4A
T30 1708-1714 GeneOrGeneProduct denotes type 2
T31 1715-1723 GeneOrGeneProduct denotes diabetes
T32 1759-1763 GeneOrGeneProduct denotes STOP

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 39-48 GeneOrGeneProduct denotes HNF4alpha
T2 92-98 GeneOrGeneProduct denotes type 2
T3 99-107 GeneOrGeneProduct denotes diabetes
T4 122-126 GeneOrGeneProduct denotes STOP
T5 159-165 GeneOrGeneProduct denotes factor
T6 174-183 GeneOrGeneProduct denotes HNF4alpha
T7 190-210 GeneOrGeneProduct denotes transcription factor
T8 260-265 GeneOrGeneProduct denotes liver
T9 355-360 GeneOrGeneProduct denotes HNF4A
T10 371-380 GeneOrGeneProduct denotes HNF4alpha
T11 449-455 GeneOrGeneProduct denotes type 2
T12 456-464 GeneOrGeneProduct denotes diabetes
T13 493-497 GeneOrGeneProduct denotes STOP
T14 606-612 GeneOrGeneProduct denotes type 2
T15 613-621 GeneOrGeneProduct denotes diabetes
T16 704-709 GeneOrGeneProduct denotes HNF4A
T17 1057-1061 GeneOrGeneProduct denotes fold
T18 1148-1156 GeneOrGeneProduct denotes diabetes
T19 1531-1537 GeneOrGeneProduct denotes type 2
T20 1538-1546 GeneOrGeneProduct denotes diabetes
T21 1667-1672 GeneOrGeneProduct denotes HNF4A
T22 1708-1714 GeneOrGeneProduct denotes type 2
T23 1715-1723 GeneOrGeneProduct denotes diabetes
T24 1759-1763 GeneOrGeneProduct denotes STOP

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 92-116 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus D003924
T2 127-132 DiseaseOrPhenotypicFeature denotes NIDDM D003924
T3 270-280 DiseaseOrPhenotypicFeature denotes pancreatic D010195
T4 413-439 DiseaseOrPhenotypicFeature denotes impaired glucose tolerance D018149
T5 441-444 DiseaseOrPhenotypicFeature denotes IGT D018149
T6 449-473 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus D003924
T7 498-503 DiseaseOrPhenotypicFeature denotes NIDDM D003924
T8 606-630 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus D003924
T9 1148-1156 DiseaseOrPhenotypicFeature denotes diabetes DISEASE
T10 1531-1555 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus D003924
T11 1708-1732 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus D003924
T12 1764-1769 DiseaseOrPhenotypicFeature denotes NIDDM D003924

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T1 39-48 GeneOrGeneProduct denotes HNF4alpha
T2 140-172 GeneOrGeneProduct denotes Hepatocyte nuclear factor 4alpha
T3 174-183 GeneOrGeneProduct denotes HNF4alpha
T4 190-210 GeneOrGeneProduct denotes transcription factor
T5 355-360 GeneOrGeneProduct denotes HNF4A
T6 371-380 GeneOrGeneProduct denotes HNF4alpha
T7 704-709 GeneOrGeneProduct denotes HNF4A
T8 1667-1672 GeneOrGeneProduct denotes HNF4A

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 92-116 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus 0005148
T2 127-132 DiseaseOrPhenotypicFeature denotes NIDDM 0005148
T3 449-473 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus 0005148
T4 498-503 DiseaseOrPhenotypicFeature denotes NIDDM 0005148
T5 606-630 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus 0005148
T6 1148-1156 DiseaseOrPhenotypicFeature denotes diabetes 0005015
T7 1345-1348 DiseaseOrPhenotypicFeature denotes men 0017169
T8 1531-1555 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus 0005148
T9 1708-1732 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus 0005148
T10 1764-1769 DiseaseOrPhenotypicFeature denotes NIDDM 0005148

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 92-116 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus D003924
T2 127-132 DiseaseOrPhenotypicFeature denotes NIDDM D003924
T3 413-439 DiseaseOrPhenotypicFeature denotes impaired glucose tolerance D018149
T4 441-444 DiseaseOrPhenotypicFeature denotes IGT D018149
T5 449-473 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus D003924
T6 498-503 DiseaseOrPhenotypicFeature denotes NIDDM D003924
T7 606-630 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus D003924
T8 1148-1156 DiseaseOrPhenotypicFeature denotes diabetes DISEASE
T9 1531-1555 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus D003924
T10 1708-1732 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus D003924
T11 1764-1769 DiseaseOrPhenotypicFeature denotes NIDDM D003924

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 92-116 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus D003924
T2 127-132 DiseaseOrPhenotypicFeature denotes NIDDM D003924
T3 413-439 DiseaseOrPhenotypicFeature denotes impaired glucose tolerance D018149
T4 441-444 DiseaseOrPhenotypicFeature denotes IGT D018149
T5 449-473 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus D003924
T6 498-503 DiseaseOrPhenotypicFeature denotes NIDDM D003924
T7 606-630 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus D003924
T8 1148-1156 DiseaseOrPhenotypicFeature denotes diabetes DISEASE
T9 1531-1555 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus D003924
T10 1708-1732 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus D003924
T11 1764-1769 DiseaseOrPhenotypicFeature denotes NIDDM D003924

LitCoin-Chemical-MeSH-CHEBI

Id Subject Object Predicate Lexical cue ID:
T1 422-429 ChemicalEntity denotes glucose D005947|http://purl.obolibrary.org/obo/CHEBI_4167|http://purl.obolibrary.org/obo/CHEBI_17234
T4 556-564 ChemicalEntity denotes acarbose D020909|http://purl.obolibrary.org/obo/CHEBI_84363|http://purl.obolibrary.org/obo/CHEBI_2376
T7 1258-1266 ChemicalEntity denotes acarbose D020909|http://purl.obolibrary.org/obo/CHEBI_84363|http://purl.obolibrary.org/obo/CHEBI_2376

LitCoin-NCBITaxon-2

Id Subject Object Predicate Lexical cue
T1 254-259 OrganismTaxon denotes human
T2 1169-1174 OrganismTaxon denotes women
T3 1345-1348 OrganismTaxon denotes men
T4 1627-1632 OrganismTaxon denotes women

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label ID:
T7 1258-1266 ChemicalEntity denotes acarbose http://purl.obolibrary.org/obo/CHEBI_2376|http://purl.obolibrary.org/obo/CHEBI_84363|D020909
T4 556-564 ChemicalEntity denotes acarbose http://purl.obolibrary.org/obo/CHEBI_2376|http://purl.obolibrary.org/obo/CHEBI_84363|D020909
T1 422-429 ChemicalEntity denotes glucose http://purl.obolibrary.org/obo/CHEBI_17234|http://purl.obolibrary.org/obo/CHEBI_4167|D005947
T8 1667-1672 GeneOrGeneProduct denotes HNF4A
T82998 704-709 GeneOrGeneProduct denotes HNF4A
T6 371-380 GeneOrGeneProduct denotes HNF4alpha
T5 355-360 GeneOrGeneProduct denotes HNF4A
T55712 190-210 GeneOrGeneProduct denotes transcription factor
T3 174-183 GeneOrGeneProduct denotes HNF4alpha
T2 140-172 GeneOrGeneProduct denotes Hepatocyte nuclear factor 4alpha
T4894 39-48 GeneOrGeneProduct denotes HNF4alpha
T11 1764-1769 DiseaseOrPhenotypicFeature denotes NIDDM D003924
T10 1708-1732 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus D003924
T9 1531-1555 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus D003924
T70112 1148-1156 DiseaseOrPhenotypicFeature denotes diabetes DISEASE
T24940 606-630 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus D003924
T79933 498-503 DiseaseOrPhenotypicFeature denotes NIDDM D003924
T5886 449-473 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus D003924
T12146 441-444 DiseaseOrPhenotypicFeature denotes IGT D018149
T62850 413-439 DiseaseOrPhenotypicFeature denotes impaired glucose tolerance D018149
T93742 127-132 DiseaseOrPhenotypicFeature denotes NIDDM D003924
T68238 92-116 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus D003924
T98449 1627-1632 OrganismTaxon denotes women
T23454 1345-1348 OrganismTaxon denotes men
T597 1169-1174 OrganismTaxon denotes women
T83649 254-259 OrganismTaxon denotes human
T50352 1416-1425 SequenceVariant denotes rs3818247
T73082 1401-1410 SequenceVariant denotes rs2071197
T62576 1390-1399 SequenceVariant denotes rs4810424
T45724 1037-1046 SequenceVariant denotes rs4810424
T71698 944-953 SequenceVariant denotes rs4810424
T25667 854-863 SequenceVariant denotes rs2144908
T10903 839-848 SequenceVariant denotes rs1884614
T82222 828-837 SequenceVariant denotes rs4810424

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
16838170-6#49#58#geners4810424 1037-1046 geners4810424 denotes rs4810424
16838170-6#160#168#diseaseC0011847 1148-1156 diseaseC0011847 denotes diabetes
16838170-6#160#168#diseaseC0011849 1148-1156 diseaseC0011849 denotes diabetes
16838170-7#51#60#geners2071197 1401-1410 geners2071197 denotes rs2071197
16838170-7#66#75#geners3818247 1416-1425 geners3818247 denotes rs3818247
16838170-7#181#205#diseaseC0011860 1531-1555 diseaseC0011860 denotes type 2 diabetes mellitus
49#58#geners4810424160#168#diseaseC0011847 16838170-6#49#58#geners4810424 16838170-6#160#168#diseaseC0011847 associated_with rs4810424,diabetes
49#58#geners4810424160#168#diseaseC0011849 16838170-6#49#58#geners4810424 16838170-6#160#168#diseaseC0011849 associated_with rs4810424,diabetes
51#60#geners2071197181#205#diseaseC0011860 16838170-7#51#60#geners2071197 16838170-7#181#205#diseaseC0011860 associated_with rs2071197,type 2 diabetes mellitus
66#75#geners3818247181#205#diseaseC0011860 16838170-7#66#75#geners3818247 16838170-7#181#205#diseaseC0011860 associated_with rs3818247,type 2 diabetes mellitus

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
16838170-0#39#48#gene3172 39-48 gene3172 denotes HNF4alpha
16838170-0#122#126#gene4135 122-126 gene4135 denotes STOP
16838170-0#92#116#diseaseC0011860 92-116 diseaseC0011860 denotes type 2 diabetes mellitus
16838170-0#127#132#diseaseC0011860 127-132 diseaseC0011860 denotes NIDDM
16838170-0#92#116#diseaseC0011860 92-116 diseaseC0011860 denotes type 2 diabetes mellitus
16838170-0#127#132#diseaseC0011860 127-132 diseaseC0011860 denotes NIDDM
16838170-2#66#71#gene3172 355-360 gene3172 denotes HNF4A
16838170-2#82#91#gene3172 371-380 gene3172 denotes HNF4alpha
16838170-2#204#208#gene4135 493-497 gene4135 denotes STOP
16838170-2#124#150#diseaseC0271650 413-439 diseaseC0271650 denotes impaired glucose tolerance
16838170-2#152#155#diseaseC0271650 441-444 diseaseC0271650 denotes IGT
16838170-2#124#150#diseaseC0271650 413-439 diseaseC0271650 denotes impaired glucose tolerance
16838170-2#152#155#diseaseC0271650 441-444 diseaseC0271650 denotes IGT
39#48#gene317292#116#diseaseC0011860 16838170-0#39#48#gene3172 16838170-0#92#116#diseaseC0011860 associated_with HNF4alpha,type 2 diabetes mellitus
39#48#gene3172127#132#diseaseC0011860 16838170-0#39#48#gene3172 16838170-0#127#132#diseaseC0011860 associated_with HNF4alpha,NIDDM
39#48#gene317292#116#diseaseC0011860 16838170-0#39#48#gene3172 16838170-0#92#116#diseaseC0011860 associated_with HNF4alpha,type 2 diabetes mellitus
39#48#gene3172127#132#diseaseC0011860 16838170-0#39#48#gene3172 16838170-0#127#132#diseaseC0011860 associated_with HNF4alpha,NIDDM
122#126#gene413592#116#diseaseC0011860 16838170-0#122#126#gene4135 16838170-0#92#116#diseaseC0011860 associated_with STOP,type 2 diabetes mellitus
122#126#gene4135127#132#diseaseC0011860 16838170-0#122#126#gene4135 16838170-0#127#132#diseaseC0011860 associated_with STOP,NIDDM
122#126#gene413592#116#diseaseC0011860 16838170-0#122#126#gene4135 16838170-0#92#116#diseaseC0011860 associated_with STOP,type 2 diabetes mellitus
122#126#gene4135127#132#diseaseC0011860 16838170-0#122#126#gene4135 16838170-0#127#132#diseaseC0011860 associated_with STOP,NIDDM
66#71#gene3172124#150#diseaseC0271650 16838170-2#66#71#gene3172 16838170-2#124#150#diseaseC0271650 associated_with HNF4A,impaired glucose tolerance
66#71#gene3172152#155#diseaseC0271650 16838170-2#66#71#gene3172 16838170-2#152#155#diseaseC0271650 associated_with HNF4A,IGT
66#71#gene3172124#150#diseaseC0271650 16838170-2#66#71#gene3172 16838170-2#124#150#diseaseC0271650 associated_with HNF4A,impaired glucose tolerance
66#71#gene3172152#155#diseaseC0271650 16838170-2#66#71#gene3172 16838170-2#152#155#diseaseC0271650 associated_with HNF4A,IGT
82#91#gene3172124#150#diseaseC0271650 16838170-2#82#91#gene3172 16838170-2#124#150#diseaseC0271650 associated_with HNF4alpha,impaired glucose tolerance
82#91#gene3172152#155#diseaseC0271650 16838170-2#82#91#gene3172 16838170-2#152#155#diseaseC0271650 associated_with HNF4alpha,IGT
82#91#gene3172124#150#diseaseC0271650 16838170-2#82#91#gene3172 16838170-2#124#150#diseaseC0271650 associated_with HNF4alpha,impaired glucose tolerance
82#91#gene3172152#155#diseaseC0271650 16838170-2#82#91#gene3172 16838170-2#152#155#diseaseC0271650 associated_with HNF4alpha,IGT
204#208#gene4135124#150#diseaseC0271650 16838170-2#204#208#gene4135 16838170-2#124#150#diseaseC0271650 associated_with STOP,impaired glucose tolerance
204#208#gene4135152#155#diseaseC0271650 16838170-2#204#208#gene4135 16838170-2#152#155#diseaseC0271650 associated_with STOP,IGT
204#208#gene4135124#150#diseaseC0271650 16838170-2#204#208#gene4135 16838170-2#124#150#diseaseC0271650 associated_with STOP,impaired glucose tolerance
204#208#gene4135152#155#diseaseC0271650 16838170-2#204#208#gene4135 16838170-2#152#155#diseaseC0271650 associated_with STOP,IGT

tmVarCorpus

Id Subject Object Predicate Lexical cue
T1 828-837 SNP:rs4810424 denotes rs4810424
T2 839-848 SNP:rs1884614 denotes rs1884614
T3 854-863 SNP:rs2144908 denotes rs2144908
T4 944-953 SNP:rs4810424 denotes rs4810424
T5 1037-1046 SNP:rs4810424 denotes rs4810424
T6 1390-1399 SNP:rs4810424 denotes rs4810424
T7 1401-1410 SNP:rs2071197 denotes rs2071197
T8 1416-1425 SNP:rs3818247 denotes rs3818247

DisGeNET

Id Subject Object Predicate Lexical cue
T0 355-360 gene:3172 denotes HNF4A
T1 413-439 disease:C0271650 denotes impaired glucose tolerance
T2 355-360 gene:3172 denotes HNF4A
T3 449-473 disease:C0011860 denotes type 2 diabetes mellitus
T4 355-360 gene:3172 denotes HNF4A
T5 498-503 disease:C0011860 denotes NIDDM
T6 371-380 gene:3172 denotes HNF4alpha
T7 413-439 disease:C0271650 denotes impaired glucose tolerance
T8 371-380 gene:3172 denotes HNF4alpha
T9 449-473 disease:C0011860 denotes type 2 diabetes mellitus
T10 493-497 gene:4135 denotes STOP
T11 413-439 disease:C0271650 denotes impaired glucose tolerance
T12 493-497 gene:4135 denotes STOP
T13 441-444 disease:C0271650 denotes IGT
T14 493-497 gene:4135 denotes STOP
T15 449-473 disease:C0011860 denotes type 2 diabetes mellitus
R1 T0 T1 associated_with HNF4A,impaired glucose tolerance
R2 T2 T3 associated_with HNF4A,type 2 diabetes mellitus
R3 T4 T5 associated_with HNF4A,NIDDM
R4 T6 T7 associated_with HNF4alpha,impaired glucose tolerance
R5 T8 T9 associated_with HNF4alpha,type 2 diabetes mellitus
R6 T10 T11 associated_with STOP,impaired glucose tolerance
R7 T12 T13 associated_with STOP,IGT
R8 T14 T15 associated_with STOP,type 2 diabetes mellitus

biored-valid-deepseek-nr-g

Id Subject Object Predicate Lexical cue
T1 39-48 GeneOrGeneProduct denotes HNF4alpha
T2 92-107 DiseaseOrPhenotypicFeature denotes type 2 diabetes
T3 108-116 DiseaseOrPhenotypicFeature denotes mellitus
T4 122-132 DiseaseOrPhenotypicFeature denotes STOP-NIDDM
T5 140-172 GeneOrGeneProduct denotes Hepatocyte nuclear factor 4alpha
T6 174-183 GeneOrGeneProduct denotes HNF4alpha
T7 254-259 OrganismTaxon denotes human
T8 355-360 GeneOrGeneProduct denotes HNF4A
T9 371-380 GeneOrGeneProduct denotes HNF4alpha
T10 413-439 DiseaseOrPhenotypicFeature denotes impaired glucose tolerance
T11 441-444 DiseaseOrPhenotypicFeature denotes IGT
T12 449-464 DiseaseOrPhenotypicFeature denotes type 2 diabetes
T13 465-473 DiseaseOrPhenotypicFeature denotes mellitus
T14 493-503 DiseaseOrPhenotypicFeature denotes STOP-NIDDM
T15 556-564 ChemicalEntity denotes acarbose
T16 577-584 ChemicalEntity denotes placebo
T17 828-837 SequenceVariant denotes rs4810424
T18 839-848 SequenceVariant denotes rs1884614
T19 854-863 SequenceVariant denotes rs2144908
T20 1037-1046 SequenceVariant denotes rs4810424
T21 1247-1254 ChemicalEntity denotes placebo
T22 1258-1266 ChemicalEntity denotes acarbose
T23 1401-1410 SequenceVariant denotes rs2071197
T24 1416-1425 SequenceVariant denotes rs3818247
T25 1531-1546 DiseaseOrPhenotypicFeature denotes type 2 diabetes
T26 1547-1555 DiseaseOrPhenotypicFeature denotes mellitus
T27 1667-1672 GeneOrGeneProduct denotes HNF4A
T28 1759-1769 DiseaseOrPhenotypicFeature denotes STOP-NIDDM

biored-valid-deepseek-nr-ng

Id Subject Object Predicate Lexical cue
T1 39-48 GeneOrGeneProduct denotes HNF4alpha
T2 92-116 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T3 140-172 GeneOrGeneProduct denotes Hepatocyte nuclear factor 4alpha
T4 174-183 GeneOrGeneProduct denotes HNF4alpha
T5 355-360 GeneOrGeneProduct denotes HNF4A
T6 371-380 GeneOrGeneProduct denotes HNF4alpha
T7 413-439 DiseaseOrPhenotypicFeature denotes impaired glucose tolerance
T8 449-473 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T9 556-564 ChemicalEntity denotes acarbose
T10 704-709 GeneOrGeneProduct denotes HNF4A
T11 828-837 SequenceVariant denotes rs4810424
T12 839-848 SequenceVariant denotes rs1884614
T13 854-863 SequenceVariant denotes rs2144908
T14 1148-1156 DiseaseOrPhenotypicFeature denotes diabetes
T15 1258-1266 ChemicalEntity denotes acarbose
T16 1390-1399 SequenceVariant denotes rs4810424
T17 1401-1410 SequenceVariant denotes rs2071197
T18 1416-1425 SequenceVariant denotes rs3818247
T19 1531-1555 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T20 1667-1672 GeneOrGeneProduct denotes HNF4A

biored-valid

Id Subject Object Predicate Lexical cue
T1 39-48 GeneOrGeneProduct denotes HNF4alpha
T2 92-116 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T3 140-172 GeneOrGeneProduct denotes Hepatocyte nuclear factor 4alpha
T4 174-183 GeneOrGeneProduct denotes HNF4alpha
T5 254-259 OrganismTaxon denotes human
T6 355-360 GeneOrGeneProduct denotes HNF4A
T7 371-380 GeneOrGeneProduct denotes HNF4alpha
T8 413-439 DiseaseOrPhenotypicFeature denotes impaired glucose tolerance
T9 441-444 DiseaseOrPhenotypicFeature denotes IGT
T10 449-473 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T11 556-564 ChemicalEntity denotes acarbose
T12 606-630 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T13 704-709 GeneOrGeneProduct denotes HNF4A
T14 828-837 SequenceVariant denotes rs4810424
T15 839-848 SequenceVariant denotes rs1884614
T16 854-863 SequenceVariant denotes rs2144908
T17 944-953 SequenceVariant denotes rs4810424
T18 1037-1046 SequenceVariant denotes rs4810424
T19 1148-1156 DiseaseOrPhenotypicFeature denotes diabetes
T20 1169-1174 OrganismTaxon denotes women
T21 1258-1266 ChemicalEntity denotes acarbose
T22 1345-1348 OrganismTaxon denotes men
T23 1390-1399 SequenceVariant denotes rs4810424
T24 1401-1410 SequenceVariant denotes rs2071197
T25 1416-1425 SequenceVariant denotes rs3818247
T26 1531-1555 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T27 1627-1632 OrganismTaxon denotes women
T28 1667-1672 GeneOrGeneProduct denotes HNF4A
T29 1708-1732 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus

biored-valid-deepseek-r-ng

Id Subject Object Predicate Lexical cue
T1 39-53 GeneOrGeneProduct denotes HNF4alpha gene
T2 92-116 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T3 174-183 GeneOrGeneProduct denotes HNF4alpha
T4 254-259 OrganismTaxon denotes human
T5 313-351 SequenceVariant denotes single nucleotide polymorphisms (SNPs)
T6 355-360 GeneOrGeneProduct denotes HNF4A
T7 413-445 DiseaseOrPhenotypicFeature denotes impaired glucose tolerance (IGT)
T8 556-564 ChemicalEntity denotes acarbose
T9 828-837 SequenceVariant denotes rs4810424
T10 839-848 SequenceVariant denotes rs1884614
T11 854-863 SequenceVariant denotes rs2144908
T12 1025-1033 SequenceVariant denotes C allele
T13 1401-1410 SequenceVariant denotes rs2071197
T14 1416-1425 SequenceVariant denotes rs3818247

biored-valid-deepseek-r-g

Id Subject Object Predicate Lexical cue
T1 0-31 SequenceVariant denotes Single nucleotide polymorphisms
T2 39-48 GeneOrGeneProduct denotes HNF4alpha
T3 92-116 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T4 140-172 GeneOrGeneProduct denotes Hepatocyte nuclear factor 4alpha
T5 174-183 GeneOrGeneProduct denotes HNF4alpha
T6 254-259 OrganismTaxon denotes human
T7 313-344 SequenceVariant denotes single nucleotide polymorphisms
T8 346-350 SequenceVariant denotes SNPs
T9 355-360 GeneOrGeneProduct denotes HNF4A
T10 413-439 DiseaseOrPhenotypicFeature denotes impaired glucose tolerance
T11 441-444 DiseaseOrPhenotypicFeature denotes IGT
T12 449-473 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T13 556-564 ChemicalEntity denotes acarbose
T14 613-621 DiseaseOrPhenotypicFeature denotes diabetes
T15 704-709 GeneOrGeneProduct denotes HNF4A
T16 828-837 SequenceVariant denotes rs4810424
T17 839-848 SequenceVariant denotes rs1884614
T18 854-863 SequenceVariant denotes rs2144908
T19 1401-1410 SequenceVariant denotes rs2071197
T20 1416-1425 SequenceVariant denotes rs3818247

biored-valid-gemini-nr-ng

Id Subject Object Predicate Lexical cue
T1 39-48 GeneOrGeneProduct denotes HNF4alpha
T2 92-116 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T3 122-132 DiseaseOrPhenotypicFeature denotes STOP-NIDDM
T4 140-172 GeneOrGeneProduct denotes Hepatocyte nuclear factor 4alpha
T5 174-183 GeneOrGeneProduct denotes HNF4alpha
T6 254-259 OrganismTaxon denotes human
T7 355-360 GeneOrGeneProduct denotes HNF4A
T8 371-380 GeneOrGeneProduct denotes HNF4alpha
T9 413-439 DiseaseOrPhenotypicFeature denotes impaired glucose tolerance
T10 441-444 DiseaseOrPhenotypicFeature denotes IGT
T11 449-473 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T12 493-503 DiseaseOrPhenotypicFeature denotes STOP-NIDDM
T13 556-564 ChemicalEntity denotes acarbose
T14 606-630 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T15 704-709 GeneOrGeneProduct denotes HNF4A
T16 828-837 SequenceVariant denotes rs4810424
T17 839-848 SequenceVariant denotes rs1884614
T18 854-863 SequenceVariant denotes rs2144908
T19 1037-1046 SequenceVariant denotes rs4810424
T20 1148-1156 DiseaseOrPhenotypicFeature denotes diabetes
T21 1258-1266 ChemicalEntity denotes acarbose
T22 1401-1410 SequenceVariant denotes rs2071197
T23 1416-1425 SequenceVariant denotes rs3818247
T24 1531-1555 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T25 1667-1672 GeneOrGeneProduct denotes HNF4A
T26 1759-1769 DiseaseOrPhenotypicFeature denotes STOP-NIDDM

PubTator4TogoVar

Id Subject Object Predicate Lexical cue resolved_to
42 828-837 SNP denotes rs4810424 tmVar:rs4810424;VariantGroup:3;CorrespondingGene:140902;RS#:4810424;CorrespondingSpecies:9606
43 839-848 SNP denotes rs1884614 tmVar:rs1884614;VariantGroup:1;RS#:1884614
44 854-863 SNP denotes rs2144908 tmVar:rs2144908;VariantGroup:4;CorrespondingGene:3172;RS#:2144908;CorrespondingSpecies:9606
45 944-953 SNP denotes rs4810424 tmVar:rs4810424;VariantGroup:3;CorrespondingGene:140902;RS#:4810424;CorrespondingSpecies:9606
46 1037-1046 SNP denotes rs4810424 tmVar:rs4810424;VariantGroup:3;CorrespondingGene:140902;RS#:4810424;CorrespondingSpecies:9606
51 1390-1399 SNP denotes rs4810424 tmVar:rs4810424;VariantGroup:3;CorrespondingGene:140902;RS#:4810424;CorrespondingSpecies:9606
52 1401-1410 SNP denotes rs2071197 tmVar:rs2071197;VariantGroup:2;CorrespondingGene:3172;RS#:2071197;CorrespondingSpecies:9606
53 1416-1425 SNP denotes rs3818247 tmVar:rs3818247;VariantGroup:0;CorrespondingGene:3172;RS#:3818247;CorrespondingSpecies:9606

biored-valid-gemini-r-ng

Id Subject Object Predicate Lexical cue
T1 0-31 SequenceVariant denotes Single nucleotide polymorphisms
T2 39-48 GeneOrGeneProduct denotes HNF4alpha
T3 92-116 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T4 140-172 GeneOrGeneProduct denotes Hepatocyte nuclear factor 4alpha
T5 174-183 GeneOrGeneProduct denotes HNF4alpha
T6 254-259 OrganismTaxon denotes human
T7 313-344 SequenceVariant denotes single nucleotide polymorphisms
T8 346-350 SequenceVariant denotes SNPs
T9 355-360 GeneOrGeneProduct denotes HNF4A
T10 371-380 GeneOrGeneProduct denotes HNF4alpha
T11 413-439 DiseaseOrPhenotypicFeature denotes impaired glucose tolerance
T12 441-444 DiseaseOrPhenotypicFeature denotes IGT
T13 449-473 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T14 556-564 ChemicalEntity denotes acarbose
T15 577-584 ChemicalEntity denotes placebo
T16 606-630 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T17 638-642 SequenceVariant denotes SNPs
T18 704-709 GeneOrGeneProduct denotes HNF4A
T19 796-800 SequenceVariant denotes SNPs
T20 828-837 SequenceVariant denotes rs4810424
T21 839-848 SequenceVariant denotes rs1884614
T22 854-863 SequenceVariant denotes rs2144908
T23 944-953 SequenceVariant denotes rs4810424
T24 1025-1033 SequenceVariant denotes C allele
T25 1037-1046 SequenceVariant denotes rs4810424
T26 1148-1156 DiseaseOrPhenotypicFeature denotes diabetes
T27 1258-1266 ChemicalEntity denotes acarbose
T28 1384-1388 SequenceVariant denotes SNPs
T29 1390-1399 SequenceVariant denotes rs4810424
T30 1401-1410 SequenceVariant denotes rs2071197
T31 1416-1425 SequenceVariant denotes rs3818247
T32 1531-1555 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T33 1659-1663 SequenceVariant denotes SNPs
T34 1667-1672 GeneOrGeneProduct denotes HNF4A

biored-valid-gemini-r-g

Id Subject Object Predicate Lexical cue
T1 39-48 GeneOrGeneProduct denotes HNF4alpha
T2 92-116 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T3 140-172 GeneOrGeneProduct denotes Hepatocyte nuclear factor 4alpha
T4 174-183 GeneOrGeneProduct denotes HNF4alpha
T5 254-259 OrganismTaxon denotes human
T6 355-360 GeneOrGeneProduct denotes HNF4A
T7 371-380 GeneOrGeneProduct denotes HNF4alpha
T8 413-439 DiseaseOrPhenotypicFeature denotes impaired glucose tolerance
T9 441-444 DiseaseOrPhenotypicFeature denotes IGT
T10 449-473 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T11 556-564 ChemicalEntity denotes acarbose
T12 704-709 GeneOrGeneProduct denotes HNF4A
T13 828-837 SequenceVariant denotes rs4810424
T14 839-848 SequenceVariant denotes rs1884614
T15 854-863 SequenceVariant denotes rs2144908
T16 1025-1033 SequenceVariant denotes C allele
T17 1037-1046 SequenceVariant denotes rs4810424
T18 1148-1156 DiseaseOrPhenotypicFeature denotes diabetes
T19 1258-1266 ChemicalEntity denotes acarbose
T20 1401-1410 SequenceVariant denotes rs2071197
T21 1416-1425 SequenceVariant denotes rs3818247
T22 1531-1555 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T23 1667-1672 GeneOrGeneProduct denotes HNF4A

biored-valid-gpt-nr-ng

Id Subject Object Predicate Lexical cue
T1 0-31 SequenceVariant denotes Single nucleotide polymorphisms
T2 39-48 GeneOrGeneProduct denotes HNF4alpha
T3 92-116 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T4 140-172 GeneOrGeneProduct denotes Hepatocyte nuclear factor 4alpha
T5 173-184 GeneOrGeneProduct denotes (HNF4alpha)
T6 254-259 OrganismTaxon denotes human
T7 313-344 SequenceVariant denotes single nucleotide polymorphisms
T8 345-351 SequenceVariant denotes (SNPs)
T9 355-361 GeneOrGeneProduct denotes HNF4A,
T10 371-381 GeneOrGeneProduct denotes HNF4alpha,
T11 413-439 DiseaseOrPhenotypicFeature denotes impaired glucose tolerance
T12 440-445 DiseaseOrPhenotypicFeature denotes (IGT)
T13 449-473 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T14 556-564 ChemicalEntity denotes acarbose
T15 606-630 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T16 638-642 SequenceVariant denotes SNPs
T17 704-709 GeneOrGeneProduct denotes HNF4A
T18 827-838 SequenceVariant denotes (rs4810424,
T19 839-848 SequenceVariant denotes rs1884614
T20 850-853 SequenceVariant denotes and
T21 854-863 SequenceVariant denotes rs2144908
T22 944-953 SequenceVariant denotes rs4810424
T23 988-994 OrganismTaxon denotes Female
T24 1025-1033 SequenceVariant denotes C allele
T25 1037-1046 SequenceVariant denotes rs4810424
T26 1148-1156 DiseaseOrPhenotypicFeature denotes diabetes
T27 1246-1254 ChemicalEntity denotes (placebo
T28 1258-1266 ChemicalEntity denotes acarbose
T29 1384-1388 SequenceVariant denotes SNPs
T30 1390-1399 SequenceVariant denotes rs4810424
T31 1401-1410 SequenceVariant denotes rs2071197
T32 1412-1415 SequenceVariant denotes and
T33 1416-1425 SequenceVariant denotes rs3818247
T34 1531-1555 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T35 1659-1663 SequenceVariant denotes SNPs
T36 1667-1672 GeneOrGeneProduct denotes HNF4A
T37 1708-1732 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus

biored-valid-gpt-nr-g

Id Subject Object Predicate Lexical cue
T1 39-53 GeneOrGeneProduct denotes HNF4alpha gene
T2 92-116 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T3 140-172 GeneOrGeneProduct denotes Hepatocyte nuclear factor 4alpha
T4 174-183 GeneOrGeneProduct denotes HNF4alpha
T5 254-259 OrganismTaxon denotes human
T6 355-360 GeneOrGeneProduct denotes HNF4A
T7 371-380 GeneOrGeneProduct denotes HNF4alpha
T8 413-439 DiseaseOrPhenotypicFeature denotes impaired glucose tolerance
T9 441-444 DiseaseOrPhenotypicFeature denotes IGT
T10 449-473 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T11 556-564 ChemicalEntity denotes acarbose
T12 606-630 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T13 704-709 GeneOrGeneProduct denotes HNF4A
T14 828-837 SequenceVariant denotes rs4810424
T15 839-848 SequenceVariant denotes rs1884614
T16 854-863 SequenceVariant denotes rs2144908
T17 944-953 SequenceVariant denotes rs4810424
T18 1025-1033 SequenceVariant denotes C allele
T19 1037-1046 SequenceVariant denotes rs4810424
T20 1148-1156 DiseaseOrPhenotypicFeature denotes diabetes
T21 1258-1266 ChemicalEntity denotes acarbose
T22 1390-1399 SequenceVariant denotes rs4810424
T23 1401-1410 SequenceVariant denotes rs2071197
T24 1416-1425 SequenceVariant denotes rs3818247
T25 1531-1555 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T26 1667-1672 GeneOrGeneProduct denotes HNF4A
T27 1708-1732 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus

biored-valid-gpt-r-g

Id Subject Object Predicate Lexical cue
T1 0-31 SequenceVariant denotes Single nucleotide polymorphisms
T2 39-53 GeneOrGeneProduct denotes HNF4alpha gene
T3 92-116 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T4 140-172 GeneOrGeneProduct denotes Hepatocyte nuclear factor 4alpha
T5 174-183 GeneOrGeneProduct denotes HNF4alpha
T6 254-259 OrganismTaxon denotes human
T7 313-344 SequenceVariant denotes single nucleotide polymorphisms
T8 346-350 SequenceVariant denotes SNPs
T9 355-360 GeneOrGeneProduct denotes HNF4A
T10 371-380 GeneOrGeneProduct denotes HNF4alpha
T11 413-439 DiseaseOrPhenotypicFeature denotes impaired glucose tolerance
T12 441-444 DiseaseOrPhenotypicFeature denotes IGT
T13 449-473 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T14 556-564 ChemicalEntity denotes acarbose
T15 606-630 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T16 638-642 SequenceVariant denotes SNPs
T17 704-709 GeneOrGeneProduct denotes HNF4A
T18 796-800 SequenceVariant denotes SNPs
T19 828-837 SequenceVariant denotes rs4810424
T20 839-848 SequenceVariant denotes rs1884614
T21 854-863 SequenceVariant denotes rs2144908
T22 944-953 SequenceVariant denotes rs4810424
T23 1025-1033 SequenceVariant denotes C allele
T24 1037-1046 SequenceVariant denotes rs4810424
T25 1148-1156 DiseaseOrPhenotypicFeature denotes diabetes
T26 1258-1266 ChemicalEntity denotes acarbose
T27 1384-1388 SequenceVariant denotes SNPs
T28 1390-1399 SequenceVariant denotes rs4810424
T29 1401-1410 SequenceVariant denotes rs2071197
T30 1416-1425 SequenceVariant denotes rs3818247
T31 1531-1555 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T32 1659-1663 SequenceVariant denotes SNPs
T33 1667-1672 GeneOrGeneProduct denotes HNF4A
T34 1708-1732 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus

biored-valid-gpt-r-ng

Id Subject Object Predicate Lexical cue
T1 0-31 SequenceVariant denotes Single nucleotide polymorphisms
T2 39-48 GeneOrGeneProduct denotes HNF4alpha
T3 92-116 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T4 140-172 GeneOrGeneProduct denotes Hepatocyte nuclear factor 4alpha
T5 174-183 GeneOrGeneProduct denotes HNF4alpha
T6 254-259 OrganismTaxon denotes human
T7 313-344 SequenceVariant denotes single nucleotide polymorphisms
T8 346-350 SequenceVariant denotes SNPs
T9 355-360 GeneOrGeneProduct denotes HNF4A
T10 371-380 GeneOrGeneProduct denotes HNF4alpha
T11 413-439 DiseaseOrPhenotypicFeature denotes impaired glucose tolerance
T12 441-444 DiseaseOrPhenotypicFeature denotes IGT
T13 449-473 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T14 556-564 ChemicalEntity denotes acarbose
T15 606-630 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T16 638-642 SequenceVariant denotes SNPs
T17 704-709 GeneOrGeneProduct denotes HNF4A
T18 796-800 SequenceVariant denotes SNPs
T19 828-837 SequenceVariant denotes rs4810424
T20 839-848 SequenceVariant denotes rs1884614
T21 854-863 SequenceVariant denotes rs2144908
T22 944-953 SequenceVariant denotes rs4810424
T23 1025-1033 SequenceVariant denotes C allele
T24 1037-1046 SequenceVariant denotes rs4810424
T25 1148-1156 DiseaseOrPhenotypicFeature denotes diabetes
T26 1258-1266 ChemicalEntity denotes acarbose
T27 1384-1388 SequenceVariant denotes SNPs
T28 1390-1399 SequenceVariant denotes rs4810424
T29 1401-1410 SequenceVariant denotes rs2071197
T30 1416-1425 SequenceVariant denotes rs3818247
T31 1531-1555 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T32 1659-1663 SequenceVariant denotes SNPs
T33 1667-1672 GeneOrGeneProduct denotes HNF4A
T34 1708-1732 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus

biored-valid-gemini-nr-g

Id Subject Object Predicate Lexical cue
T1 0-31 SequenceVariant denotes Single nucleotide polymorphisms
T2 39-48 GeneOrGeneProduct denotes HNF4alpha
T3 92-116 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T4 140-172 GeneOrGeneProduct denotes Hepatocyte nuclear factor 4alpha
T5 174-183 GeneOrGeneProduct denotes HNF4alpha
T6 313-344 SequenceVariant denotes single nucleotide polymorphisms
T7 346-350 SequenceVariant denotes SNPs
T8 355-360 GeneOrGeneProduct denotes HNF4A
T9 371-380 GeneOrGeneProduct denotes HNF4alpha
T10 413-439 DiseaseOrPhenotypicFeature denotes impaired glucose tolerance
T11 441-444 DiseaseOrPhenotypicFeature denotes IGT
T12 449-473 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T13 556-564 ChemicalEntity denotes acarbose
T14 638-642 SequenceVariant denotes SNPs
T15 704-709 GeneOrGeneProduct denotes HNF4A
T16 828-837 SequenceVariant denotes rs4810424
T17 839-848 SequenceVariant denotes rs1884614
T18 854-863 SequenceVariant denotes rs2144908
T19 1037-1046 SequenceVariant denotes rs4810424
T20 1148-1156 DiseaseOrPhenotypicFeature denotes diabetes
T21 1258-1266 ChemicalEntity denotes acarbose
T22 1269-1276 DiseaseOrPhenotypicFeature denotes smoking
T23 1384-1388 SequenceVariant denotes SNPs
T24 1401-1410 SequenceVariant denotes rs2071197
T25 1416-1425 SequenceVariant denotes rs3818247
T26 1531-1555 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T27 1667-1672 GeneOrGeneProduct denotes HNF4A

biored-valid-gpt-r-m

Id Subject Object Predicate Lexical cue
T1 39-48 GeneOrGeneProduct denotes HNF4alpha
T2 92-116 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T3 140-172 GeneOrGeneProduct denotes Hepatocyte nuclear factor 4alpha
T4 174-183 GeneOrGeneProduct denotes HNF4alpha
T5 254-259 OrganismTaxon denotes human
T6 355-360 GeneOrGeneProduct denotes HNF4A
T7 371-380 GeneOrGeneProduct denotes HNF4alpha
T8 413-439 DiseaseOrPhenotypicFeature denotes impaired glucose tolerance
T9 441-444 DiseaseOrPhenotypicFeature denotes IGT
T10 449-473 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T11 477-485 OrganismTaxon denotes subjects
T12 556-564 ChemicalEntity denotes acarbose
T13 606-630 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T14 704-709 GeneOrGeneProduct denotes HNF4A
T15 828-837 SequenceVariant denotes rs4810424
T16 839-848 SequenceVariant denotes rs1884614
T17 854-863 SequenceVariant denotes rs2144908
T18 944-953 SequenceVariant denotes rs4810424
T19 1025-1033 SequenceVariant denotes C allele
T20 1037-1046 SequenceVariant denotes rs4810424
T21 1148-1156 DiseaseOrPhenotypicFeature denotes diabetes
T22 1258-1266 ChemicalEntity denotes acarbose
T23 1390-1399 SequenceVariant denotes rs4810424
T24 1401-1410 SequenceVariant denotes rs2071197
T25 1416-1425 SequenceVariant denotes rs3818247
T26 1531-1555 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T27 1667-1672 GeneOrGeneProduct denotes HNF4A
T28 1708-1732 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T29 1743-1751 OrganismTaxon denotes subjects

biored-valid-gemini-r-m

Id Subject Object Predicate Lexical cue
T1 0-31 SequenceVariant denotes Single nucleotide polymorphisms
T2 39-48 GeneOrGeneProduct denotes HNF4alpha
T3 92-116 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T4 140-172 GeneOrGeneProduct denotes Hepatocyte nuclear factor 4alpha
T5 174-183 GeneOrGeneProduct denotes HNF4alpha
T6 254-259 OrganismTaxon denotes human
T7 313-344 SequenceVariant denotes single nucleotide polymorphisms
T8 346-350 SequenceVariant denotes SNPs
T9 355-360 GeneOrGeneProduct denotes HNF4A
T10 371-380 GeneOrGeneProduct denotes HNF4alpha
T11 413-439 DiseaseOrPhenotypicFeature denotes impaired glucose tolerance
T12 441-444 DiseaseOrPhenotypicFeature denotes IGT
T13 449-473 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T14 477-485 OrganismTaxon denotes subjects
T15 556-564 ChemicalEntity denotes acarbose
T16 606-630 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T17 638-642 SequenceVariant denotes SNPs
T18 704-709 GeneOrGeneProduct denotes HNF4A
T19 828-837 SequenceVariant denotes rs4810424
T20 839-848 SequenceVariant denotes rs1884614
T21 854-863 SequenceVariant denotes rs2144908
T22 944-953 SequenceVariant denotes rs4810424
T23 995-1003 OrganismTaxon denotes carriers
T24 1025-1033 SequenceVariant denotes C allele
T25 1148-1156 DiseaseOrPhenotypicFeature denotes diabetes
T26 1169-1174 OrganismTaxon denotes women
T27 1216-1219 OrganismTaxon denotes men
T28 1258-1266 ChemicalEntity denotes acarbose
T29 1384-1388 SequenceVariant denotes SNPs
T30 1390-1399 SequenceVariant denotes rs4810424
T31 1401-1410 SequenceVariant denotes rs2071197
T32 1416-1425 SequenceVariant denotes rs3818247
T33 1531-1555 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T34 1587-1599 SequenceVariant denotes risk alleles
T35 1627-1632 OrganismTaxon denotes women
T36 1667-1672 GeneOrGeneProduct denotes HNF4A
T37 1743-1751 OrganismTaxon denotes subjects

biored-valid-deepseek-r-m

Id Subject Object Predicate Lexical cue
T1 39-48 GeneOrGeneProduct denotes HNF4alpha
T2 92-116 DiseaseOrPhenotypicFeature denotes type 2 diabetes mellitus
T3 140-172 GeneOrGeneProduct denotes Hepatocyte nuclear factor 4alpha
T4 174-183 GeneOrGeneProduct denotes HNF4alpha
T5 254-259 OrganismTaxon denotes human
T6 355-360 GeneOrGeneProduct denotes HNF4A
T7 413-439 DiseaseOrPhenotypicFeature denotes impaired glucose tolerance
T8 441-444 DiseaseOrPhenotypicFeature denotes IGT
T9 456-464 DiseaseOrPhenotypicFeature denotes diabetes
T10 556-564 ChemicalEntity denotes acarbose
T11 828-837 SequenceVariant denotes rs4810424
T12 839-848 SequenceVariant denotes rs1884614
T13 854-863 SequenceVariant denotes rs2144908
T14 1401-1410 SequenceVariant denotes rs2071197
T15 1416-1425 SequenceVariant denotes rs3818247

PubTatorOnTogoVar

Id Subject Object Predicate Lexical cue resolved_to
42 828-837 SNP denotes rs4810424 tmVar:rs4810424;VariantGroup:3;CorrespondingGene:140902;RS#:4810424;CorrespondingSpecies:9606
43 839-848 SNP denotes rs1884614 tmVar:rs1884614;VariantGroup:1;RS#:1884614
44 854-863 SNP denotes rs2144908 tmVar:rs2144908;VariantGroup:4;CorrespondingGene:3172;RS#:2144908;CorrespondingSpecies:9606
45 944-953 SNP denotes rs4810424 tmVar:rs4810424;VariantGroup:3;CorrespondingGene:140902;RS#:4810424;CorrespondingSpecies:9606
46 1037-1046 SNP denotes rs4810424 tmVar:rs4810424;VariantGroup:3;CorrespondingGene:140902;RS#:4810424;CorrespondingSpecies:9606
51 1390-1399 SNP denotes rs4810424 tmVar:rs4810424;VariantGroup:3;CorrespondingGene:140902;RS#:4810424;CorrespondingSpecies:9606
52 1401-1410 SNP denotes rs2071197 tmVar:rs2071197;VariantGroup:2;CorrespondingGene:3172;RS#:2071197;CorrespondingSpecies:9606
53 1416-1425 SNP denotes rs3818247 tmVar:rs3818247;VariantGroup:0;CorrespondingGene:3172;RS#:3818247;CorrespondingSpecies:9606
T1 828-837 SNP denotes rs4810424 tmVar:rs4810424;VariantGroup:3;CorrespondingGene:140902;RS#:4810424;CorrespondingSpecies:9606
T2 839-848 SNP denotes rs1884614 tmVar:rs1884614;VariantGroup:1;RS#:1884614
T3 854-863 SNP denotes rs2144908 tmVar:rs2144908;VariantGroup:4;CorrespondingGene:3172;RS#:2144908;CorrespondingSpecies:9606
T4 944-953 SNP denotes rs4810424 tmVar:rs4810424;VariantGroup:3;CorrespondingGene:140902;RS#:4810424;CorrespondingSpecies:9606
T5 1037-1046 SNP denotes rs4810424 tmVar:rs4810424;VariantGroup:3;CorrespondingGene:140902;RS#:4810424;CorrespondingSpecies:9606
T6 1390-1399 SNP denotes rs4810424 tmVar:rs4810424;VariantGroup:3;CorrespondingGene:140902;RS#:4810424;CorrespondingSpecies:9606
T7 1401-1410 SNP denotes rs2071197 tmVar:rs2071197;VariantGroup:2;CorrespondingGene:3172;RS#:2071197;CorrespondingSpecies:9606
T8 1416-1425 SNP denotes rs3818247 tmVar:rs3818247;VariantGroup:0;CorrespondingGene:3172;RS#:3818247;CorrespondingSpecies:9606