PubMed:21163864 JSONTXT 28 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue #label ID:
T51700 4-9 SequenceVariant denotes M235T
T1 30-45 ChemicalEntity denotes angiotensinogen http://purl.obolibrary.org/obo/CHEBI_2720
T17276 30-45 GeneOrGeneProduct denotes angiotensinogen
T20650 67-75 OrganismTaxon denotes patients
T82531 79-106 DiseaseOrPhenotypicFeature denotes hypertrophic cardiomyopathy D002312
T22764 122-149 DiseaseOrPhenotypicFeature denotes Hypertrophic cardiomyopathy D002312
T29946 151-154 DiseaseOrPhenotypicFeature denotes HCM D002312
T95815 206-221 DiseaseOrPhenotypicFeature denotes cardiac disease D006331
T80 327-332 SequenceVariant denotes T704C
T2 363-378 ChemicalEntity denotes angiotensinogen http://purl.obolibrary.org/obo/CHEBI_2720
T32452 363-378 GeneOrGeneProduct denotes angiotensinogen
T3 380-383 ChemicalEntity denotes AGT http://purl.obolibrary.org/obo/CHEBI_2720
T11450 380-383 GeneOrGeneProduct denotes AGT
T56346 395-398 DiseaseOrPhenotypicFeature denotes HCM D002312
T6 493-496 DiseaseOrPhenotypicFeature denotes HCM D002312
T48987 510-537 DiseaseOrPhenotypicFeature denotes hypertrophic cardiomyopathy D002312
T92499 539-543 DiseaseOrPhenotypicFeature denotes SHCM DISEASE
T74733 552-588 DiseaseOrPhenotypicFeature denotes familial hypertrophic cardiomyopathy D024741
T10 590-594 DiseaseOrPhenotypicFeature denotes FHCM DISEASE
T51459 597-605 OrganismTaxon denotes patients
T11 673-685 DiseaseOrPhenotypicFeature denotes hypertension D006973
T12 690-718 DiseaseOrPhenotypicFeature denotes left ventricular hypertrophy D017379
T4 825-828 ChemicalEntity denotes AGT http://purl.obolibrary.org/obo/CHEBI_2720
T80293 825-828 GeneOrGeneProduct denotes AGT
T5 862-872 ChemicalEntity denotes methionine http://purl.obolibrary.org/obo/CHEBI_16811|http://purl.obolibrary.org/obo/CHEBI_64558
T7 876-885 ChemicalEntity denotes threonine http://purl.obolibrary.org/obo/CHEBI_26986
T66735 913-918 SequenceVariant denotes M235T
T8 1054-1059 ChemicalEntity denotes SfaNI ChemicalEntity
T13 1202-1206 DiseaseOrPhenotypicFeature denotes SHCM DISEASE
T74231 1207-1215 OrganismTaxon denotes patients
T14 1281-1285 DiseaseOrPhenotypicFeature denotes FHCM DISEASE
T9 1344-1347 ChemicalEntity denotes AGT http://purl.obolibrary.org/obo/CHEBI_2720
T3742 1344-1347 GeneOrGeneProduct denotes AGT
T15 1386-1390 DiseaseOrPhenotypicFeature denotes SHCM DISEASE
T16 1516-1520 DiseaseOrPhenotypicFeature denotes FHCM DISEASE