PubMed:19319147 JSONTXT 24 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue #label ID:
T80370 42-52 DiseaseOrPhenotypicFeature denotes hemorrhage D006470
T69342 65-70 OrganismTaxon denotes mouse
T1 80-88 ChemicalEntity denotes warfarin http://purl.obolibrary.org/obo/CHEBI_10033|D014859
T76063 100-124 DiseaseOrPhenotypicFeature denotes intracerebral hemorrhage D002543
T3 126-134 ChemicalEntity denotes Warfarin http://purl.obolibrary.org/obo/CHEBI_10033|D014859
T4613 146-170 DiseaseOrPhenotypicFeature denotes intracerebral hemorrhage D002543
T4 174-177 DiseaseOrPhenotypicFeature denotes ICH DISEASE
T48694 199-205 DiseaseOrPhenotypicFeature denotes stroke D020521
T31365 260-263 DiseaseOrPhenotypicFeature denotes ICH DISEASE
T67382 273-278 OrganismTaxon denotes mouse
T30175 348-353 OrganismTaxon denotes human
T5 354-365 ChemicalEntity denotes prothrombin http://purl.obolibrary.org/obo/CHEBI_8583
T4882 354-365 GeneOrGeneProduct denotes prothrombin
T6 387-390 ChemicalEntity denotes PCC ChemicalEntity
T60085 439-443 OrganismTaxon denotes mice
T7 462-470 ChemicalEntity denotes warfarin http://purl.obolibrary.org/obo/CHEBI_10033|D014859
T25854 622-627 OrganismTaxon denotes human
T9 628-631 ChemicalEntity denotes PCC ChemicalEntity
T51508 668-672 OrganismTaxon denotes mice
T10 710-721 ChemicalEntity denotes collagenase ChemicalEntity|D017364
T57988 749-759 DiseaseOrPhenotypicFeature denotes hemorrhage D006470
T12 848-851 ChemicalEntity denotes PCC ChemicalEntity
T8 920-930 DiseaseOrPhenotypicFeature denotes hemorrhage D006470
T13 1002-1012 ChemicalEntity denotes hemoglobin http://purl.obolibrary.org/obo/CHEBI_35143
T2 1002-1012 GeneOrGeneProduct denotes hemoglobin
T14 1069-1072 ChemicalEntity denotes PCC ChemicalEntity
T25701 1201-1205 OrganismTaxon denotes mice
T64851 1222-1231 DiseaseOrPhenotypicFeature denotes hematomas D006406
T15 1312-1315 ChemicalEntity denotes PCC ChemicalEntity
T16 1363-1366 ChemicalEntity denotes PCC ChemicalEntity
T24843 1408-1411 DiseaseOrPhenotypicFeature denotes ICH DISEASE
T9166 1551-1556 OrganismTaxon denotes human
T11 1559-1562 DiseaseOrPhenotypicFeature denotes ICH DISEASE