> top > docs > PubMed:16252083 > spans > 568-953 > annotations

PubMed:16252083 / 568-953 JSONTXT

Annnotations TAB JSON ListView MergeView

PubTator4TogoVar

Id Subject Object Predicate Lexical cue proteinmutation
16252083_0 154-191 ProteinMutation denotes Asn --> Ser substitution at codon 127 rs17217772
16252083_1 278-309 ProteinMutation denotes Gly --> Asp change at codon 322 rs4987188

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T5 0-385 Sentence denotes We performed a case-control study to test the association between two polymorphisms in the hMSH2 gene: an A --> G transition at 127 position producing an Asn --> Ser substitution at codon 127 (the Asn127Ser polymorphism) and a G --> A transition at 1032 position resulting in a Gly --> Asp change at codon 322 (the Gly322Asp polymorphism) and breast cancer risk and cancer progression.

LitCoin-entities-OrganismTaxon-PD

Id Subject Object Predicate Lexical cue db_id
T1 182-187 OrganismTaxon denotes codon NCBItxid:79338
T2 300-305 OrganismTaxon denotes codon NCBItxid:79338

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
2445 91-96 GeneOrGeneProduct denotes hMSH2 NCBIGene:4436
2446 106-140 SequenceVariant denotes A --> G transition at 127 position DBSNP:rs17217772
2447 154-191 SequenceVariant denotes Asn --> Ser substitution at codon 127 DBSNP:rs17217772
2448 197-206 SequenceVariant denotes Asn127Ser DBSNP:rs17217772
2449 227-262 SequenceVariant denotes G --> A transition at 1032 position DBSNP:rs4987188
2450 278-309 SequenceVariant denotes Gly --> Asp change at codon 322 DBSNP:rs4987188
2451 315-324 SequenceVariant denotes Gly322Asp DBSNP:rs4987188
2452 343-356 DiseaseOrPhenotypicFeature denotes breast cancer MESH:D001943
2453 366-372 DiseaseOrPhenotypicFeature denotes cancer MESH:D009369

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T8 343-356 DiseaseOrPhenotypicFeature denotes breast cancer 0007254
T9 350-356 DiseaseOrPhenotypicFeature denotes cancer 0004992
T10 366-372 DiseaseOrPhenotypicFeature denotes cancer 0004992

LitCoin-SeqVar

Id Subject Object Predicate Lexical cue
T1 197-206 SequenceVariant denotes Asn127Ser
T2 315-324 SequenceVariant denotes Gly322Asp

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T12 15-19 GeneOrGeneProduct denotes case
T13 37-41 GeneOrGeneProduct denotes test
T14 91-96 GeneOrGeneProduct denotes hMSH2
T15 103-113 GeneOrGeneProduct denotes an A --> G
T16 154-157 GeneOrGeneProduct denotes Asn
T17 162-165 GeneOrGeneProduct denotes Ser
T18 273-277 GeneOrGeneProduct denotes in a

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T8 91-96 GeneOrGeneProduct denotes hMSH2

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T7 343-356 DiseaseOrPhenotypicFeature denotes breast cancer D001943
T8 366-372 DiseaseOrPhenotypicFeature denotes cancer D009369

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T4 91-96 GeneOrGeneProduct denotes hMSH2

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T7 343-356 DiseaseOrPhenotypicFeature denotes breast cancer 0007254|0004989

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T7 343-356 DiseaseOrPhenotypicFeature denotes breast cancer D001943
T8 366-372 DiseaseOrPhenotypicFeature denotes cancer D009369

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T7 343-356 DiseaseOrPhenotypicFeature denotes breast cancer D001943
T8 366-372 DiseaseOrPhenotypicFeature denotes cancer D009369

LitCoin-Chemical-MeSH-CHEBI

Id Subject Object Predicate Lexical cue ID:
T1 154-157 ChemicalEntity denotes Asn http://purl.obolibrary.org/obo/CHEBI_50347|http://purl.obolibrary.org/obo/CHEBI_22653|http://purl.obolibrary.org/obo/CHEBI_17196
T4 162-165 ChemicalEntity denotes Ser http://purl.obolibrary.org/obo/CHEBI_29999|http://purl.obolibrary.org/obo/CHEBI_17115
T6 278-281 ChemicalEntity denotes Gly http://purl.obolibrary.org/obo/CHEBI_15428
T7 286-289 ChemicalEntity denotes Asp http://purl.obolibrary.org/obo/CHEBI_29958|http://purl.obolibrary.org/obo/CHEBI_22660|http://purl.obolibrary.org/obo/CHEBI_17053

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label ID:
T7 286-289 ChemicalEntity denotes Asp http://purl.obolibrary.org/obo/CHEBI_17053|http://purl.obolibrary.org/obo/CHEBI_22660|http://purl.obolibrary.org/obo/CHEBI_29958
T6 278-281 ChemicalEntity denotes Gly http://purl.obolibrary.org/obo/CHEBI_15428
T4 162-165 ChemicalEntity denotes Ser http://purl.obolibrary.org/obo/CHEBI_17115|http://purl.obolibrary.org/obo/CHEBI_29999
T1 154-157 ChemicalEntity denotes Asn http://purl.obolibrary.org/obo/CHEBI_17196|http://purl.obolibrary.org/obo/CHEBI_22653|http://purl.obolibrary.org/obo/CHEBI_50347
T37804 91-96 GeneOrGeneProduct denotes hMSH2
T8 366-372 DiseaseOrPhenotypicFeature denotes cancer D009369
T26934 343-356 DiseaseOrPhenotypicFeature denotes breast cancer D001943
T5825 315-324 SequenceVariant denotes Gly322Asp
T64918 197-206 SequenceVariant denotes Asn127Ser

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
16252083-4#315#324#geners4987188 315-324 geners4987188 denotes Gly322Asp
16252083-4#197#206#geners17217772 197-206 geners17217772 denotes Asn127Ser
16252083-4#366#384#diseaseC0178874 366-384 diseaseC0178874 denotes cancer progression
16252083-4#343#356#diseaseC0006142 343-356 diseaseC0006142 denotes breast cancer
16252083-4#343#356#diseaseC0678222 343-356 diseaseC0678222 denotes breast cancer
16252083-4#366#384#diseaseC0178874 366-384 diseaseC0178874 denotes cancer progression
315#324#geners4987188366#384#diseaseC0178874 16252083-4#315#324#geners4987188 16252083-4#366#384#diseaseC0178874 associated_with Gly322Asp,cancer progression
315#324#geners4987188343#356#diseaseC0006142 16252083-4#315#324#geners4987188 16252083-4#343#356#diseaseC0006142 associated_with Gly322Asp,breast cancer
315#324#geners4987188343#356#diseaseC0678222 16252083-4#315#324#geners4987188 16252083-4#343#356#diseaseC0678222 associated_with Gly322Asp,breast cancer
315#324#geners4987188366#384#diseaseC0178874 16252083-4#315#324#geners4987188 16252083-4#366#384#diseaseC0178874 associated_with Gly322Asp,cancer progression
197#206#geners17217772366#384#diseaseC0178874 16252083-4#197#206#geners17217772 16252083-4#366#384#diseaseC0178874 associated_with Asn127Ser,cancer progression
197#206#geners17217772343#356#diseaseC0006142 16252083-4#197#206#geners17217772 16252083-4#343#356#diseaseC0006142 associated_with Asn127Ser,breast cancer
197#206#geners17217772343#356#diseaseC0678222 16252083-4#197#206#geners17217772 16252083-4#343#356#diseaseC0678222 associated_with Asn127Ser,breast cancer
197#206#geners17217772366#384#diseaseC0178874 16252083-4#197#206#geners17217772 16252083-4#366#384#diseaseC0178874 associated_with Asn127Ser,cancer progression

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
16252083-4#91#96#gene4436 91-96 gene4436 denotes hMSH2
16252083-4#366#384#diseaseC0178874 366-384 diseaseC0178874 denotes cancer progression
91#96#gene4436366#384#diseaseC0178874 16252083-4#91#96#gene4436 16252083-4#366#384#diseaseC0178874 associated_with hMSH2,cancer progression

tmVarCorpus

Id Subject Object Predicate Lexical cue
T1 106-140 DNAMutation:|SUB|A|CODON127|G denotes A --> G transition at 127 position
T2 154-191 ProteinMutation:p|SUB|N|127|S denotes Asn --> Ser substitution at codon 127
T3 197-206 ProteinMutation:p|SUB|N|127|S denotes Asn127Ser
T4 227-262 DNAMutation:g|SUB|G|1032|A denotes G --> A transition at 1032 position
T5 278-309 ProteinMutation:p|SUB|G|322|D denotes Gly --> Asp change at codon 322
T6 315-324 ProteinMutation:p|SUB|G|322|D denotes Gly322Asp