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TEST-DiseaseOrPhenotypicFeature

Id Subject Object Predicate Lexical cue #label
T1 337-349 DiseaseOrPhenotypicFeature denotes hypertension D006973
T2 519-531 DiseaseOrPhenotypicFeature denotes hypertension D006973
T3 590-602 DiseaseOrPhenotypicFeature denotes hypertension D006973
T4 786-808 DiseaseOrPhenotypicFeature denotes essential hypertension D000075222
T5 1561-1573 DiseaseOrPhenotypicFeature denotes hypertension D006973

TEST-ChemicalEntity

Id Subject Object Predicate Lexical cue ID:
T1 41-58 ChemicalEntity denotes mineralocorticoid http://purl.obolibrary.org/obo/CHEBI_25354
T2 254-271 ChemicalEntity denotes mineralocorticoid http://purl.obolibrary.org/obo/CHEBI_25354
T3 1683-1700 ChemicalEntity denotes mineralocorticoid http://purl.obolibrary.org/obo/CHEBI_25354

TEST-OrganismTaxon

Id Subject Object Predicate Lexical cue
T1 576-584 OrganismTaxon denotes patients
T2 888-896 OrganismTaxon denotes patients

Test-SequenceVariant

Id Subject Object Predicate Lexical cue
T1 27-32 SequenceVariant denotes F826Y
T2 187-192 SequenceVariant denotes S810L
T3 611-616 SequenceVariant denotes S810L
T4 671-676 SequenceVariant denotes S810L
T5 734-739 SequenceVariant denotes S810L
T6 872-877 SequenceVariant denotes F826Y
T7 1010-1015 SequenceVariant denotes L809L
T8 1022-1027 SequenceVariant denotes F826Y
T9 1123-1128 SequenceVariant denotes F826Y
T10 1315-1320 SequenceVariant denotes F826Y
T11 1628-1633 SequenceVariant denotes F826Y

Test-GeneOrGeneProduct

Id Subject Object Predicate Lexical cue
T1 41-67 GeneOrGeneProduct denotes mineralocorticoid receptor
T2 254-280 GeneOrGeneProduct denotes mineralocorticoid receptor
T3 292-298 GeneOrGeneProduct denotes symbol
T4 299-304 GeneOrGeneProduct denotes NR3C2
T5 1683-1709 GeneOrGeneProduct denotes mineralocorticoid receptor

Test-merged-2

Id Subject Object Predicate Lexical cue #label ID:
T68309 27-32 SequenceVariant denotes F826Y
T64764 187-192 SequenceVariant denotes S810L
T90304 611-616 SequenceVariant denotes S810L
T44069 671-676 SequenceVariant denotes S810L
T3446 734-739 SequenceVariant denotes S810L
T6 872-877 SequenceVariant denotes F826Y
T7 1010-1015 SequenceVariant denotes L809L
T8 1022-1027 SequenceVariant denotes F826Y
T9 1123-1128 SequenceVariant denotes F826Y
T10 1315-1320 SequenceVariant denotes F826Y
T11 1628-1633 SequenceVariant denotes F826Y
T10440 41-58 ChemicalEntity denotes mineralocorticoid http://purl.obolibrary.org/obo/CHEBI_25354
T86532 254-271 ChemicalEntity denotes mineralocorticoid http://purl.obolibrary.org/obo/CHEBI_25354
T21280 1683-1700 ChemicalEntity denotes mineralocorticoid http://purl.obolibrary.org/obo/CHEBI_25354
T66595 41-67 GeneOrGeneProduct denotes mineralocorticoid receptor
T26815 254-280 GeneOrGeneProduct denotes mineralocorticoid receptor
T48459 292-298 GeneOrGeneProduct denotes symbol
T47981 299-304 GeneOrGeneProduct denotes NR3C2
T6939 1683-1709 GeneOrGeneProduct denotes mineralocorticoid receptor
T3315 576-584 OrganismTaxon denotes patients
T66871 888-896 OrganismTaxon denotes patients
T1 337-349 DiseaseOrPhenotypicFeature denotes hypertension D006973
T2 519-531 DiseaseOrPhenotypicFeature denotes hypertension D006973
T3 590-602 DiseaseOrPhenotypicFeature denotes hypertension D006973
T4 786-808 DiseaseOrPhenotypicFeature denotes essential hypertension D000075222
T5 1561-1573 DiseaseOrPhenotypicFeature denotes hypertension D006973

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
16419642-3#126#131#geners41511344 671-676 geners41511344 denotes S810L
16419642-3#189#194#geners41511344 734-739 geners41511344 denotes S810L
16419642-3#66#71#geners41511344 611-616 geners41511344 denotes S810L
16419642-3#45#57#diseaseC0020538 590-602 diseaseC0020538 denotes hypertension
16419642-3#241#263#diseaseC0085580 786-808 diseaseC0085580 denotes essential hypertension
16419642-3#45#57#diseaseC0020538 590-602 diseaseC0020538 denotes hypertension
16419642-3#241#263#diseaseC0085580 786-808 diseaseC0085580 denotes essential hypertension
16419642-3#45#57#diseaseC0020538 590-602 diseaseC0020538 denotes hypertension
16419642-3#241#263#diseaseC0085580 786-808 diseaseC0085580 denotes essential hypertension
16419642-7#23#28#geners13306592 1315-1320 geners13306592 denotes F826Y
16419642-7#269#281#diseaseC0020538 1561-1573 diseaseC0020538 denotes hypertension
126#131#geners4151134445#57#diseaseC0020538 16419642-3#126#131#geners41511344 16419642-3#45#57#diseaseC0020538 associated_with S810L,hypertension
126#131#geners41511344241#263#diseaseC0085580 16419642-3#126#131#geners41511344 16419642-3#241#263#diseaseC0085580 associated_with S810L,essential hypertension
126#131#geners4151134445#57#diseaseC0020538 16419642-3#126#131#geners41511344 16419642-3#45#57#diseaseC0020538 associated_with S810L,hypertension
126#131#geners41511344241#263#diseaseC0085580 16419642-3#126#131#geners41511344 16419642-3#241#263#diseaseC0085580 associated_with S810L,essential hypertension
126#131#geners4151134445#57#diseaseC0020538 16419642-3#126#131#geners41511344 16419642-3#45#57#diseaseC0020538 associated_with S810L,hypertension
126#131#geners41511344241#263#diseaseC0085580 16419642-3#126#131#geners41511344 16419642-3#241#263#diseaseC0085580 associated_with S810L,essential hypertension
189#194#geners4151134445#57#diseaseC0020538 16419642-3#189#194#geners41511344 16419642-3#45#57#diseaseC0020538 associated_with S810L,hypertension
189#194#geners41511344241#263#diseaseC0085580 16419642-3#189#194#geners41511344 16419642-3#241#263#diseaseC0085580 associated_with S810L,essential hypertension
189#194#geners4151134445#57#diseaseC0020538 16419642-3#189#194#geners41511344 16419642-3#45#57#diseaseC0020538 associated_with S810L,hypertension
189#194#geners41511344241#263#diseaseC0085580 16419642-3#189#194#geners41511344 16419642-3#241#263#diseaseC0085580 associated_with S810L,essential hypertension
189#194#geners4151134445#57#diseaseC0020538 16419642-3#189#194#geners41511344 16419642-3#45#57#diseaseC0020538 associated_with S810L,hypertension
189#194#geners41511344241#263#diseaseC0085580 16419642-3#189#194#geners41511344 16419642-3#241#263#diseaseC0085580 associated_with S810L,essential hypertension
66#71#geners4151134445#57#diseaseC0020538 16419642-3#66#71#geners41511344 16419642-3#45#57#diseaseC0020538 associated_with S810L,hypertension
66#71#geners41511344241#263#diseaseC0085580 16419642-3#66#71#geners41511344 16419642-3#241#263#diseaseC0085580 associated_with S810L,essential hypertension
66#71#geners4151134445#57#diseaseC0020538 16419642-3#66#71#geners41511344 16419642-3#45#57#diseaseC0020538 associated_with S810L,hypertension
66#71#geners41511344241#263#diseaseC0085580 16419642-3#66#71#geners41511344 16419642-3#241#263#diseaseC0085580 associated_with S810L,essential hypertension
66#71#geners4151134445#57#diseaseC0020538 16419642-3#66#71#geners41511344 16419642-3#45#57#diseaseC0020538 associated_with S810L,hypertension
66#71#geners41511344241#263#diseaseC0085580 16419642-3#66#71#geners41511344 16419642-3#241#263#diseaseC0085580 associated_with S810L,essential hypertension
23#28#geners13306592269#281#diseaseC0020538 16419642-7#23#28#geners13306592 16419642-7#269#281#diseaseC0020538 associated_with F826Y,hypertension

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
16419642-1#112#138#gene4306 254-280 gene4306 denotes mineralocorticoid receptor
16419642-1#157#162#gene4306 299-304 gene4306 denotes NR3C2
16419642-1#195#207#diseaseC0020538 337-349 diseaseC0020538 denotes hypertension
112#138#gene4306195#207#diseaseC0020538 16419642-1#112#138#gene4306 16419642-1#195#207#diseaseC0020538 associated_with mineralocorticoid receptor,hypertension
157#162#gene4306195#207#diseaseC0020538 16419642-1#157#162#gene4306 16419642-1#195#207#diseaseC0020538 associated_with NR3C2,hypertension

tmVarCorpus

Id Subject Object Predicate Lexical cue
T1 27-32 ProteinMutation:p|SUB|F|826|Y denotes F826Y
T2 187-192 ProteinMutation:p|SUB|S|810|L denotes S810L
T3 611-616 ProteinMutation:p|SUB|S|810|L denotes S810L
T4 671-676 ProteinMutation:p|SUB|S|810|L denotes S810L
T5 734-739 ProteinMutation:p|SUB|S|810|L denotes S810L
T6 872-877 ProteinMutation:p|SUB|F|826|Y denotes F826Y
T7 1010-1015 ProteinMutation:p|SUB|L|809|L denotes L809L
T8 1022-1027 ProteinMutation:p|SUB|F|826|Y denotes F826Y
T9 1123-1128 ProteinMutation:p|SUB|F|826|Y denotes F826Y
T10 1315-1320 ProteinMutation:p|SUB|F|826|Y denotes F826Y
T11 1628-1633 ProteinMutation:p|SUB|F|826|Y denotes F826Y

DisGeNET

Id Subject Object Predicate Lexical cue
T0 254-280 gene:4306 denotes mineralocorticoid receptor
T1 337-349 disease:C0020538 denotes hypertension
T2 299-304 gene:4306 denotes NR3C2
T3 337-349 disease:C0020538 denotes hypertension
R1 T0 T1 associated_with mineralocorticoid receptor,hypertension
R2 T2 T3 associated_with NR3C2,hypertension

biored-valid-deepseek-nr-g

Id Subject Object Predicate Lexical cue
T1 27-32 SequenceVariant denotes F826Y
T2 41-72 GeneOrGeneProduct denotes mineralocorticoid receptor gene
T3 76-98 DiseaseOrPhenotypicFeature denotes Japanese hypertensives
T4 187-192 SequenceVariant denotes S810L
T5 193-216 SequenceVariant denotes amino acid substitution
T6 224-246 GeneOrGeneProduct denotes hormone-binding domain
T7 254-280 GeneOrGeneProduct denotes mineralocorticoid receptor
T8 282-284 GeneOrGeneProduct denotes MR
T9 299-304 GeneOrGeneProduct denotes NR3C2
T10 325-349 DiseaseOrPhenotypicFeature denotes early-onset hypertension
T11 535-543 OrganismTaxon denotes Japanese
T12 567-584 OrganismTaxon denotes Japanese patients
T13 611-616 SequenceVariant denotes S810L
T14 629-635 GeneOrGeneProduct denotes exon 6
T15 643-645 GeneOrGeneProduct denotes MR
T16 693-705 DiseaseOrPhenotypicFeature denotes hypertensive
T17 734-744 SequenceVariant denotes S810L does
T18 786-808 DiseaseOrPhenotypicFeature denotes essential hypertension
T19 812-820 OrganismTaxon denotes Japanese
T20 872-877 SequenceVariant denotes F826Y
T21 942-973 SequenceVariant denotes single nucleotide polymorphisms
T22 1010-1015 SequenceVariant denotes L809L
T23 1022-1027 SequenceVariant denotes F826Y
T24 1055-1057 GeneOrGeneProduct denotes MR
T25 1058-1080 GeneOrGeneProduct denotes hormone-binding domain
T26 1123-1128 SequenceVariant denotes F826Y
T27 1179-1191 DiseaseOrPhenotypicFeature denotes hypertensive
T28 1199-1211 DiseaseOrPhenotypicFeature denotes normotensive
T29 1228-1256 OrganismTaxon denotes general population (n=3,655)
T30 1315-1320 SequenceVariant denotes F826Y
T31 1683-1709 GeneOrGeneProduct denotes mineralocorticoid receptor

biored-valid-deepseek-nr-ng

Id Subject Object Predicate Lexical cue
T1 27-32 SequenceVariant denotes F826Y
T2 41-67 GeneOrGeneProduct denotes mineralocorticoid receptor
T3 76-98 DiseaseOrPhenotypicFeature denotes Japanese hypertensives
T4 187-192 SequenceVariant denotes S810L
T5 254-280 GeneOrGeneProduct denotes mineralocorticoid receptor
T6 282-304 GeneOrGeneProduct denotes MR, locus symbol NR3C2
T7 337-349 DiseaseOrPhenotypicFeature denotes hypertension
T8 519-531 DiseaseOrPhenotypicFeature denotes hypertension
T9 535-543 OrganismTaxon denotes Japanese
T10 567-584 OrganismTaxon denotes Japanese patients
T11 590-602 DiseaseOrPhenotypicFeature denotes hypertension
T12 611-616 SequenceVariant denotes S810L
T13 629-635 SequenceVariant denotes exon 6
T14 643-645 GeneOrGeneProduct denotes MR
T15 796-808 DiseaseOrPhenotypicFeature denotes hypertension
T16 872-877 SequenceVariant denotes F826Y
T17 1022-1027 SequenceVariant denotes F826Y
T18 1055-1057 GeneOrGeneProduct denotes MR
T19 1123-1128 SequenceVariant denotes F826Y
T20 1219-1246 OrganismTaxon denotes Japanese general population
T21 1683-1709 GeneOrGeneProduct denotes mineralocorticoid receptor

biored-valid

Id Subject Object Predicate Lexical cue
T1 27-32 SequenceVariant denotes F826Y
T2 41-67 GeneOrGeneProduct denotes mineralocorticoid receptor
T3 85-98 DiseaseOrPhenotypicFeature denotes hypertensives
T4 187-192 SequenceVariant denotes S810L
T5 254-280 GeneOrGeneProduct denotes mineralocorticoid receptor
T6 282-284 GeneOrGeneProduct denotes MR
T7 299-304 GeneOrGeneProduct denotes NR3C2
T8 337-349 DiseaseOrPhenotypicFeature denotes hypertension
T9 519-531 DiseaseOrPhenotypicFeature denotes hypertension
T10 576-584 OrganismTaxon denotes patients
T11 590-602 DiseaseOrPhenotypicFeature denotes hypertension
T12 611-616 SequenceVariant denotes S810L
T13 643-645 GeneOrGeneProduct denotes MR
T14 671-676 SequenceVariant denotes S810L
T15 693-705 DiseaseOrPhenotypicFeature denotes hypertensive
T16 734-739 SequenceVariant denotes S810L
T17 786-808 DiseaseOrPhenotypicFeature denotes essential hypertension
T18 872-877 SequenceVariant denotes F826Y
T19 888-896 OrganismTaxon denotes patients
T20 1010-1015 SequenceVariant denotes L809L
T21 1022-1027 SequenceVariant denotes F826Y
T22 1055-1057 GeneOrGeneProduct denotes MR
T23 1123-1128 SequenceVariant denotes F826Y
T24 1179-1192 DiseaseOrPhenotypicFeature denotes hypertensives
T25 1315-1320 SequenceVariant denotes F826Y
T26 1337-1349 DiseaseOrPhenotypicFeature denotes hypertensive
T27 1380-1392 DiseaseOrPhenotypicFeature denotes hypertensive
T28 1561-1573 DiseaseOrPhenotypicFeature denotes hypertension
T29 1628-1633 SequenceVariant denotes F826Y
T30 1683-1709 GeneOrGeneProduct denotes mineralocorticoid receptor
T31 1821-1823 GeneOrGeneProduct denotes MR

biored-valid-deepseek-r-ng

Id Subject Object Predicate Lexical cue
T1 27-32 SequenceVariant denotes F826Y
T2 41-72 GeneOrGeneProduct denotes mineralocorticoid receptor gene
T3 187-192 SequenceVariant denotes S810L
T4 282-284 GeneOrGeneProduct denotes MR
T5 299-304 GeneOrGeneProduct denotes NR3C2
T6 337-349 DiseaseOrPhenotypicFeature denotes hypertension
T7 590-602 DiseaseOrPhenotypicFeature denotes hypertension
T8 643-645 GeneOrGeneProduct denotes MR
T9 786-808 DiseaseOrPhenotypicFeature denotes essential hypertension
T10 872-877 SequenceVariant denotes F826Y
T11 1010-1015 SequenceVariant denotes L809L

biored-valid-deepseek-r-g

Id Subject Object Predicate Lexical cue
T1 27-32 SequenceVariant denotes F826Y
T2 41-72 GeneOrGeneProduct denotes mineralocorticoid receptor gene
T3 85-98 DiseaseOrPhenotypicFeature denotes hypertensives
T4 121-140 DiseaseOrPhenotypicFeature denotes clinical phenotypes
T5 187-192 SequenceVariant denotes S810L
T6 254-280 GeneOrGeneProduct denotes mineralocorticoid receptor
T7 282-284 GeneOrGeneProduct denotes MR
T8 299-304 GeneOrGeneProduct denotes NR3C2
T9 337-349 DiseaseOrPhenotypicFeature denotes hypertension
T10 519-531 DiseaseOrPhenotypicFeature denotes hypertension
T11 643-645 GeneOrGeneProduct denotes MR
T12 693-705 DiseaseOrPhenotypicFeature denotes hypertensive
T13 796-808 DiseaseOrPhenotypicFeature denotes hypertension
T14 872-877 SequenceVariant denotes F826Y
T15 1010-1015 SequenceVariant denotes L809L
T16 1055-1057 GeneOrGeneProduct denotes MR
T17 1179-1192 DiseaseOrPhenotypicFeature denotes hypertensives

biored-valid-gemini-nr-ng

Id Subject Object Predicate Lexical cue
T1 27-32 SequenceVariant denotes F826Y
T2 41-72 GeneOrGeneProduct denotes mineralocorticoid receptor gene
T3 85-98 DiseaseOrPhenotypicFeature denotes hypertensives
T4 187-192 SequenceVariant denotes S810L
T5 254-280 GeneOrGeneProduct denotes mineralocorticoid receptor
T6 282-284 GeneOrGeneProduct denotes MR
T7 299-304 GeneOrGeneProduct denotes NR3C2
T8 337-349 DiseaseOrPhenotypicFeature denotes hypertension
T9 373-382 DiseaseOrPhenotypicFeature denotes pregnancy
T10 519-531 DiseaseOrPhenotypicFeature denotes hypertension
T11 611-616 SequenceVariant denotes S810L
T12 643-645 GeneOrGeneProduct denotes MR
T13 786-808 DiseaseOrPhenotypicFeature denotes essential hypertension
T14 872-877 SequenceVariant denotes F826Y
T15 1010-1015 SequenceVariant denotes L809L
T16 1022-1027 SequenceVariant denotes F826Y
T17 1055-1057 GeneOrGeneProduct denotes MR
T18 1179-1192 DiseaseOrPhenotypicFeature denotes hypertensives
T19 1199-1212 DiseaseOrPhenotypicFeature denotes normotensives
T20 1315-1320 SequenceVariant denotes F826Y
T21 1561-1573 DiseaseOrPhenotypicFeature denotes hypertension
T22 1683-1709 GeneOrGeneProduct denotes mineralocorticoid receptor
T23 1821-1823 GeneOrGeneProduct denotes MR

biored-valid-gemini-r-ng

Id Subject Object Predicate Lexical cue
T1 8-25 DiseaseOrPhenotypicFeature denotes missense mutation
T2 27-32 SequenceVariant denotes F826Y
T3 41-72 GeneOrGeneProduct denotes mineralocorticoid receptor gene
T4 76-84 OrganismTaxon denotes Japanese
T5 85-98 DiseaseOrPhenotypicFeature denotes hypertensives
T6 121-140 DiseaseOrPhenotypicFeature denotes clinical phenotypes
T7 144-169 DiseaseOrPhenotypicFeature denotes gain-of-function mutation
T8 187-216 SequenceVariant denotes S810L amino acid substitution
T9 254-280 GeneOrGeneProduct denotes mineralocorticoid receptor
T10 282-284 GeneOrGeneProduct denotes MR
T11 299-304 GeneOrGeneProduct denotes NR3C2
T12 325-349 DiseaseOrPhenotypicFeature denotes early-onset hypertension
T13 447-465 DiseaseOrPhenotypicFeature denotes missense mutations
T14 519-531 DiseaseOrPhenotypicFeature denotes hypertension
T15 535-543 OrganismTaxon denotes Japanese
T16 611-625 SequenceVariant denotes S810L mutation
T17 643-645 GeneOrGeneProduct denotes MR
T18 671-676 SequenceVariant denotes S810L
T19 693-705 DiseaseOrPhenotypicFeature denotes hypertensive
T20 786-808 DiseaseOrPhenotypicFeature denotes essential hypertension
T21 812-820 OrganismTaxon denotes Japanese
T22 853-870 DiseaseOrPhenotypicFeature denotes missense mutation
T23 872-877 SequenceVariant denotes F826Y
T24 902-920 DiseaseOrPhenotypicFeature denotes heterozygous state
T25 942-973 DiseaseOrPhenotypicFeature denotes single nucleotide polymorphisms
T26 989-1008 DiseaseOrPhenotypicFeature denotes synonymous mutation
T27 1010-1015 SequenceVariant denotes L809L
T28 1022-1036 SequenceVariant denotes F826Y mutation
T29 1055-1057 GeneOrGeneProduct denotes MR
T30 1123-1137 SequenceVariant denotes F826Y mutation
T31 1179-1192 DiseaseOrPhenotypicFeature denotes hypertensives
T32 1199-1212 DiseaseOrPhenotypicFeature denotes normotensives
T33 1219-1227 OrganismTaxon denotes Japanese
T34 1337-1349 DiseaseOrPhenotypicFeature denotes hypertensive
T35 1561-1573 DiseaseOrPhenotypicFeature denotes hypertension
T36 1628-1642 SequenceVariant denotes F826Y mutation
T37 1683-1709 GeneOrGeneProduct denotes mineralocorticoid receptor
T38 1725-1742 DiseaseOrPhenotypicFeature denotes missense mutation
T39 1778-1797 DiseaseOrPhenotypicFeature denotes clinical phenotypes
T40 1821-1823 GeneOrGeneProduct denotes MR

biored-valid-gemini-r-g

Id Subject Object Predicate Lexical cue
T1 27-32 SequenceVariant denotes F826Y
T2 41-72 GeneOrGeneProduct denotes mineralocorticoid receptor gene
T3 76-84 OrganismTaxon denotes Japanese
T4 85-98 DiseaseOrPhenotypicFeature denotes hypertensives
T5 187-192 SequenceVariant denotes S810L
T6 254-280 GeneOrGeneProduct denotes mineralocorticoid receptor
T7 282-284 GeneOrGeneProduct denotes MR
T8 299-304 GeneOrGeneProduct denotes NR3C2
T9 337-349 DiseaseOrPhenotypicFeature denotes hypertension
T10 519-531 DiseaseOrPhenotypicFeature denotes hypertension
T11 535-543 OrganismTaxon denotes Japanese
T12 611-616 SequenceVariant denotes S810L
T13 643-645 GeneOrGeneProduct denotes MR
T14 671-676 SequenceVariant denotes S810L
T15 693-705 DiseaseOrPhenotypicFeature denotes hypertensive
T16 786-808 DiseaseOrPhenotypicFeature denotes essential hypertension
T17 812-820 OrganismTaxon denotes Japanese
T18 872-877 SequenceVariant denotes F826Y
T19 1010-1015 SequenceVariant denotes L809L
T20 1022-1027 SequenceVariant denotes F826Y
T21 1055-1057 GeneOrGeneProduct denotes MR
T22 1179-1192 DiseaseOrPhenotypicFeature denotes hypertensives
T23 1219-1227 OrganismTaxon denotes Japanese
T24 1315-1320 SequenceVariant denotes F826Y
T25 1337-1349 DiseaseOrPhenotypicFeature denotes hypertensive
T26 1561-1573 DiseaseOrPhenotypicFeature denotes hypertension
T27 1628-1633 SequenceVariant denotes F826Y
T28 1683-1709 GeneOrGeneProduct denotes mineralocorticoid receptor
T29 1821-1823 GeneOrGeneProduct denotes MR

biored-valid-gpt-nr-ng

Id Subject Object Predicate Lexical cue
T1 27-32 SequenceVariant denotes F826Y
T2 41-72 GeneOrGeneProduct denotes mineralocorticoid receptor gene
T3 85-98 DiseaseOrPhenotypicFeature denotes hypertensives
T4 187-192 SequenceVariant denotes S810L
T5 254-280 GeneOrGeneProduct denotes mineralocorticoid receptor
T6 282-284 GeneOrGeneProduct denotes MR
T7 299-304 GeneOrGeneProduct denotes NR3C2
T8 337-349 DiseaseOrPhenotypicFeature denotes hypertension
T9 519-531 DiseaseOrPhenotypicFeature denotes hypertension
T10 590-602 DiseaseOrPhenotypicFeature denotes hypertension
T11 611-616 SequenceVariant denotes S810L
T12 643-645 GeneOrGeneProduct denotes MR
T13 671-676 SequenceVariant denotes S810L
T14 734-739 SequenceVariant denotes S810L
T15 786-808 DiseaseOrPhenotypicFeature denotes essential hypertension
T16 872-877 SequenceVariant denotes F826Y
T17 1010-1015 SequenceVariant denotes L809L
T18 1022-1027 SequenceVariant denotes F826Y
T19 1055-1057 GeneOrGeneProduct denotes MR
T20 1102-1108 ChemicalEntity denotes ligand
T21 1123-1128 SequenceVariant denotes F826Y
T22 1179-1192 DiseaseOrPhenotypicFeature denotes hypertensives
T23 1199-1212 DiseaseOrPhenotypicFeature denotes normotensives
T24 1315-1320 SequenceVariant denotes F826Y
T25 1337-1349 DiseaseOrPhenotypicFeature denotes hypertensive
T26 1418-1430 DiseaseOrPhenotypicFeature denotes normotensive
T27 1561-1573 DiseaseOrPhenotypicFeature denotes hypertension
T28 1628-1633 SequenceVariant denotes F826Y
T29 1683-1709 GeneOrGeneProduct denotes mineralocorticoid receptor
T30 1821-1823 GeneOrGeneProduct denotes MR

biored-valid-gpt-nr-g

Id Subject Object Predicate Lexical cue
T1 27-32 SequenceVariant denotes F826Y
T2 41-72 GeneOrGeneProduct denotes mineralocorticoid receptor gene
T3 85-98 DiseaseOrPhenotypicFeature denotes hypertensives
T4 187-192 SequenceVariant denotes S810L
T5 254-280 GeneOrGeneProduct denotes mineralocorticoid receptor
T6 282-284 GeneOrGeneProduct denotes MR
T7 299-304 GeneOrGeneProduct denotes NR3C2
T8 337-349 DiseaseOrPhenotypicFeature denotes hypertension
T9 519-531 DiseaseOrPhenotypicFeature denotes hypertension
T10 590-602 DiseaseOrPhenotypicFeature denotes hypertension
T11 611-616 SequenceVariant denotes S810L
T12 643-645 GeneOrGeneProduct denotes MR
T13 671-676 SequenceVariant denotes S810L
T14 693-705 DiseaseOrPhenotypicFeature denotes hypertensive
T15 734-739 SequenceVariant denotes S810L
T16 786-808 DiseaseOrPhenotypicFeature denotes essential hypertension
T17 1010-1015 SequenceVariant denotes L809L
T18 1022-1027 SequenceVariant denotes F826Y
T19 1055-1057 GeneOrGeneProduct denotes MR
T20 1123-1128 SequenceVariant denotes F826Y
T21 1179-1192 DiseaseOrPhenotypicFeature denotes hypertensives
T22 1315-1320 SequenceVariant denotes F826Y
T23 1337-1349 DiseaseOrPhenotypicFeature denotes hypertensive
T24 1561-1573 DiseaseOrPhenotypicFeature denotes hypertension
T25 1683-1709 GeneOrGeneProduct denotes mineralocorticoid receptor
T26 1821-1823 GeneOrGeneProduct denotes MR

biored-valid-gpt-r-ng

Id Subject Object Predicate Lexical cue
T1 27-32 SequenceVariant denotes F826Y
T2 41-72 GeneOrGeneProduct denotes mineralocorticoid receptor gene
T3 85-98 DiseaseOrPhenotypicFeature denotes hypertensives
T4 121-140 DiseaseOrPhenotypicFeature denotes clinical phenotypes
T5 187-192 SequenceVariant denotes S810L
T6 254-280 GeneOrGeneProduct denotes mineralocorticoid receptor
T7 282-284 GeneOrGeneProduct denotes MR
T8 299-304 GeneOrGeneProduct denotes NR3C2
T9 325-349 DiseaseOrPhenotypicFeature denotes early-onset hypertension
T10 373-382 DiseaseOrPhenotypicFeature denotes pregnancy
T11 519-531 DiseaseOrPhenotypicFeature denotes hypertension
T12 611-616 SequenceVariant denotes S810L
T13 643-645 GeneOrGeneProduct denotes MR
T14 671-676 SequenceVariant denotes S810L
T15 693-705 DiseaseOrPhenotypicFeature denotes hypertensive
T16 734-739 SequenceVariant denotes S810L
T17 786-808 DiseaseOrPhenotypicFeature denotes essential hypertension
T18 872-877 SequenceVariant denotes F826Y
T19 1010-1015 SequenceVariant denotes L809L
T20 1022-1027 SequenceVariant denotes F826Y
T21 1055-1057 GeneOrGeneProduct denotes MR
T22 1123-1128 SequenceVariant denotes F826Y
T23 1179-1192 DiseaseOrPhenotypicFeature denotes hypertensives
T24 1199-1212 DiseaseOrPhenotypicFeature denotes normotensives
T25 1315-1320 SequenceVariant denotes F826Y
T26 1337-1349 DiseaseOrPhenotypicFeature denotes hypertensive
T27 1418-1430 DiseaseOrPhenotypicFeature denotes normotensive
T28 1561-1573 DiseaseOrPhenotypicFeature denotes hypertension
T29 1628-1633 SequenceVariant denotes F826Y
T30 1683-1709 GeneOrGeneProduct denotes mineralocorticoid receptor
T31 1778-1797 DiseaseOrPhenotypicFeature denotes clinical phenotypes
T32 1821-1823 GeneOrGeneProduct denotes MR

biored-valid-gpt-r-g

Id Subject Object Predicate Lexical cue
T1 8-25 SequenceVariant denotes missense mutation
T2 27-32 SequenceVariant denotes F826Y
T3 41-72 GeneOrGeneProduct denotes mineralocorticoid receptor gene
T4 85-98 DiseaseOrPhenotypicFeature denotes hypertensives
T5 144-169 SequenceVariant denotes gain-of-function mutation
T6 187-192 SequenceVariant denotes S810L
T7 193-216 SequenceVariant denotes amino acid substitution
T8 254-280 GeneOrGeneProduct denotes mineralocorticoid receptor
T9 282-284 GeneOrGeneProduct denotes MR
T10 299-304 GeneOrGeneProduct denotes NR3C2
T11 337-349 DiseaseOrPhenotypicFeature denotes hypertension
T12 447-465 SequenceVariant denotes missense mutations
T13 519-531 DiseaseOrPhenotypicFeature denotes hypertension
T14 590-602 DiseaseOrPhenotypicFeature denotes hypertension
T15 611-616 SequenceVariant denotes S810L
T16 643-645 GeneOrGeneProduct denotes MR
T17 671-676 SequenceVariant denotes S810L
T18 693-705 DiseaseOrPhenotypicFeature denotes hypertensive
T19 734-739 SequenceVariant denotes S810L
T20 786-808 DiseaseOrPhenotypicFeature denotes essential hypertension
T21 853-870 SequenceVariant denotes missense mutation
T22 872-877 SequenceVariant denotes F826Y
T23 942-973 SequenceVariant denotes single nucleotide polymorphisms
T24 989-1008 SequenceVariant denotes synonymous mutation
T25 1010-1015 SequenceVariant denotes L809L
T26 1022-1027 SequenceVariant denotes F826Y
T27 1055-1057 GeneOrGeneProduct denotes MR
T28 1123-1128 SequenceVariant denotes F826Y
T29 1179-1192 DiseaseOrPhenotypicFeature denotes hypertensives
T30 1315-1320 SequenceVariant denotes F826Y
T31 1337-1349 DiseaseOrPhenotypicFeature denotes hypertensive
T32 1561-1573 DiseaseOrPhenotypicFeature denotes hypertension
T33 1628-1633 SequenceVariant denotes F826Y
T34 1683-1709 GeneOrGeneProduct denotes mineralocorticoid receptor
T35 1725-1742 SequenceVariant denotes missense mutation
T36 1821-1823 GeneOrGeneProduct denotes MR

biored-valid-gemini-nr-g

Id Subject Object Predicate Lexical cue
T1 8-25 SequenceVariant denotes missense mutation
T2 27-32 SequenceVariant denotes F826Y
T3 41-72 GeneOrGeneProduct denotes mineralocorticoid receptor gene
T4 76-84 OrganismTaxon denotes Japanese
T5 85-98 DiseaseOrPhenotypicFeature denotes hypertensives
T6 144-169 SequenceVariant denotes gain-of-function mutation
T7 187-192 SequenceVariant denotes S810L
T8 193-216 SequenceVariant denotes amino acid substitution
T9 254-280 GeneOrGeneProduct denotes mineralocorticoid receptor
T10 282-284 GeneOrGeneProduct denotes MR
T11 299-304 GeneOrGeneProduct denotes NR3C2
T12 325-349 DiseaseOrPhenotypicFeature denotes early-onset hypertension
T13 373-382 DiseaseOrPhenotypicFeature denotes pregnancy
T14 447-465 SequenceVariant denotes missense mutations
T15 519-531 DiseaseOrPhenotypicFeature denotes hypertension
T16 535-543 OrganismTaxon denotes Japanese
T17 611-616 SequenceVariant denotes S810L
T18 617-625 SequenceVariant denotes mutation
T19 643-645 GeneOrGeneProduct denotes MR
T20 671-676 SequenceVariant denotes S810L
T21 693-705 DiseaseOrPhenotypicFeature denotes hypertensive
T22 786-808 DiseaseOrPhenotypicFeature denotes essential hypertension
T23 812-820 OrganismTaxon denotes Japanese
T24 853-1016 SequenceVariant denotes missense mutation, F826Y, in three patients in a heterozygous state, in addition to four single nucleotide polymorphisms, including one synonymous mutation (L809L)
T25 1022-1027 SequenceVariant denotes F826Y
T26 1055-1057 GeneOrGeneProduct denotes MR
T27 1123-1128 SequenceVariant denotes F826Y
T28 1129-1137 SequenceVariant denotes mutation
T29 1179-1192 DiseaseOrPhenotypicFeature denotes hypertensives
T30 1199-1212 DiseaseOrPhenotypicFeature denotes normotensives
T31 1219-1227 OrganismTaxon denotes Japanese
T32 1321-1329 SequenceVariant denotes mutation
T33 1528-1536 SequenceVariant denotes mutation
T34 1561-1573 DiseaseOrPhenotypicFeature denotes hypertension
T35 1628-1633 SequenceVariant denotes F826Y
T36 1683-1709 GeneOrGeneProduct denotes mineralocorticoid receptor
T37 1725-1742 SequenceVariant denotes missense mutation
T38 1821-1823 GeneOrGeneProduct denotes MR

biored-valid-gpt-r-m

Id Subject Object Predicate Lexical cue
T1 27-32 SequenceVariant denotes F826Y
T2 41-67 GeneOrGeneProduct denotes mineralocorticoid receptor
T3 85-98 DiseaseOrPhenotypicFeature denotes hypertensives
T4 187-192 SequenceVariant denotes S810L
T5 254-280 GeneOrGeneProduct denotes mineralocorticoid receptor
T6 282-284 GeneOrGeneProduct denotes MR
T7 299-304 GeneOrGeneProduct denotes NR3C2
T8 337-349 DiseaseOrPhenotypicFeature denotes hypertension
T9 519-531 DiseaseOrPhenotypicFeature denotes hypertension
T10 576-584 OrganismTaxon denotes patients
T11 590-602 DiseaseOrPhenotypicFeature denotes hypertension
T12 611-616 SequenceVariant denotes S810L
T13 643-645 GeneOrGeneProduct denotes MR
T14 671-676 SequenceVariant denotes S810L
T15 693-705 DiseaseOrPhenotypicFeature denotes hypertensive
T16 734-739 SequenceVariant denotes S810L
T17 796-808 DiseaseOrPhenotypicFeature denotes hypertension
T18 872-877 SequenceVariant denotes F826Y
T19 888-896 OrganismTaxon denotes patients
T20 1010-1015 SequenceVariant denotes L809L
T21 1022-1027 SequenceVariant denotes F826Y
T22 1055-1057 GeneOrGeneProduct denotes MR
T23 1123-1128 SequenceVariant denotes F826Y
T24 1179-1192 DiseaseOrPhenotypicFeature denotes hypertensives
T25 1315-1320 SequenceVariant denotes F826Y
T26 1337-1349 DiseaseOrPhenotypicFeature denotes hypertensive
T27 1561-1573 DiseaseOrPhenotypicFeature denotes hypertension
T28 1628-1633 SequenceVariant denotes F826Y
T29 1683-1709 GeneOrGeneProduct denotes mineralocorticoid receptor
T30 1821-1823 GeneOrGeneProduct denotes MR

biored-valid-gemini-r-m

Id Subject Object Predicate Lexical cue
T1 8-25 SequenceVariant denotes missense mutation
T2 27-32 SequenceVariant denotes F826Y
T3 41-72 GeneOrGeneProduct denotes mineralocorticoid receptor gene
T4 76-84 OrganismTaxon denotes Japanese
T5 85-98 DiseaseOrPhenotypicFeature denotes hypertensives
T6 144-169 SequenceVariant denotes gain-of-function mutation
T7 187-192 SequenceVariant denotes S810L
T8 254-280 GeneOrGeneProduct denotes mineralocorticoid receptor
T9 282-284 GeneOrGeneProduct denotes MR
T10 299-304 GeneOrGeneProduct denotes NR3C2
T11 325-349 DiseaseOrPhenotypicFeature denotes early-onset hypertension
T12 447-465 SequenceVariant denotes missense mutations
T13 519-531 DiseaseOrPhenotypicFeature denotes hypertension
T14 535-543 OrganismTaxon denotes Japanese
T15 576-584 OrganismTaxon denotes patients
T16 611-625 SequenceVariant denotes S810L mutation
T17 643-645 GeneOrGeneProduct denotes MR
T18 689-692 OrganismTaxon denotes our
T19 693-705 DiseaseOrPhenotypicFeature denotes hypertensive
T20 786-808 DiseaseOrPhenotypicFeature denotes essential hypertension
T21 812-820 OrganismTaxon denotes Japanese
T22 853-870 SequenceVariant denotes missense mutation
T23 872-877 SequenceVariant denotes F826Y
T24 888-896 OrganismTaxon denotes patients
T25 937-973 SequenceVariant denotes four single nucleotide polymorphisms
T26 989-1016 SequenceVariant denotes synonymous mutation (L809L)
T27 1022-1036 SequenceVariant denotes F826Y mutation
T28 1055-1057 GeneOrGeneProduct denotes MR
T29 1123-1137 SequenceVariant denotes F826Y mutation
T30 1164-1175 OrganismTaxon denotes individuals
T31 1179-1192 DiseaseOrPhenotypicFeature denotes hypertensives
T32 1199-1211 DiseaseOrPhenotypicFeature denotes normotensive
T33 1219-1227 OrganismTaxon denotes Japanese
T34 1561-1573 DiseaseOrPhenotypicFeature denotes hypertension
T35 1628-1642 SequenceVariant denotes F826Y mutation
T36 1683-1709 GeneOrGeneProduct denotes mineralocorticoid receptor
T37 1720-1742 SequenceVariant denotes this missense mutation
T38 1821-1823 GeneOrGeneProduct denotes MR

biored-valid-deepseek-r-m

Id Subject Object Predicate Lexical cue
T1 27-32 SequenceVariant denotes F826Y
T2 41-67 GeneOrGeneProduct denotes mineralocorticoid receptor
T3 85-98 DiseaseOrPhenotypicFeature denotes hypertensives
T4 187-192 SequenceVariant denotes S810L
T5 282-284 GeneOrGeneProduct denotes MR
T6 299-304 GeneOrGeneProduct denotes NR3C2
T7 337-349 DiseaseOrPhenotypicFeature denotes hypertension
T8 786-808 DiseaseOrPhenotypicFeature denotes essential hypertension
T9 1010-1015 SequenceVariant denotes L809L