PubMed:19208385 / 0-167 JSONTXT 20 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function

Id Subject Object Predicate Lexical cue mondo_id
T1 0-32 DiseaseOrPhenotypicFeature denotes Osteogenesis imperfecta type III 0009804
T2 38-61 DiseaseOrPhenotypicFeature denotes intracranial hemorrhage 0005049
T3 66-79 DiseaseOrPhenotypicFeature denotes brachydactyly 0021004|0017424
T5 128-151 DiseaseOrPhenotypicFeature denotes Osteogenesis imperfecta 0019019
T6 153-155 DiseaseOrPhenotypicFeature denotes OI 0019019