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PubMed:16419642 JSONTXT

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PubTator4TogoVar

Id Subject Object Predicate Lexical cue proteinmutation
16419642_0 27-32 ProteinMutation denotes F826Y rs13306592
16419642_1 872-877 ProteinMutation denotes F826Y rs13306592
16419642_2 1010-1015 ProteinMutation denotes L809L rs145670736
16419642_3 1022-1027 ProteinMutation denotes F826Y rs13306592
16419642_4 1123-1128 ProteinMutation denotes F826Y rs13306592
16419642_5 1315-1320 ProteinMutation denotes F826Y rs13306592
16419642_6 1628-1633 ProteinMutation denotes F826Y rs13306592

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

Test-merged

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

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