PubMed:19208385 JSONTXT 31 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue #label ID:
T35891 0-32 DiseaseOrPhenotypicFeature denotes Osteogenesis imperfecta type III C536044
T85622 38-61 DiseaseOrPhenotypicFeature denotes intracranial hemorrhage D020300
T39072 66-79 DiseaseOrPhenotypicFeature denotes brachydactyly D059327
T57517 120-126 GeneOrGeneProduct denotes COL1A2
T73081 128-151 DiseaseOrPhenotypicFeature denotes Osteogenesis imperfecta D010013
T88966 153-155 DiseaseOrPhenotypicFeature denotes OI D010013
T47980 172-185 DiseaseOrPhenotypicFeature denotes bone disorder DISEASE
T7 203-212 DiseaseOrPhenotypicFeature denotes fractures DISEASE
T8 226-232 DiseaseOrPhenotypicFeature denotes trauma D014947
T9 234-257 DiseaseOrPhenotypicFeature denotes Intracranial hemorrhage D020300
T10 297-299 DiseaseOrPhenotypicFeature denotes OI D010013
T82831 300-308 OrganismTaxon denotes patients
T48265 333-341 OrganismTaxon denotes patients
T11 406-408 DiseaseOrPhenotypicFeature denotes OI D010013
T12 431-454 DiseaseOrPhenotypicFeature denotes intracranial hemorrhage D020300
T13 475-488 DiseaseOrPhenotypicFeature denotes brachydactyly D059327
T14 493-508 DiseaseOrPhenotypicFeature denotes nail hypoplasia DISEASE
T12992 526-534 OrganismTaxon denotes patients
T15 536-538 DiseaseOrPhenotypicFeature denotes OI D010013
T1 553-560 ChemicalEntity denotes glycine http://purl.obolibrary.org/obo/CHEBI_15428|http://purl.obolibrary.org/obo/CHEBI_29947|http://purl.obolibrary.org/obo/CHEBI_57305
T2 596-602 GeneOrGeneProduct denotes COL1A2
T4 634-641 ChemicalEntity denotes carboxy http://purl.obolibrary.org/obo/CHEBI_46883
T5 692-700 ChemicalEntity denotes collagen http://purl.obolibrary.org/obo/CHEBI_3815
T3 692-721 GeneOrGeneProduct denotes collagen type I alpha 2 chain
T6 787-795 ChemicalEntity denotes collagen http://purl.obolibrary.org/obo/CHEBI_3815
T78675 787-816 GeneOrGeneProduct denotes collagen type I alpha 2 chain
T16 838-863 DiseaseOrPhenotypicFeature denotes abnormal limb development DISEASE
T17 881-889 DiseaseOrPhenotypicFeature denotes bleeding D006470