PubMed:1709636 JSONTXT 31 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T1 102-117 SpecificDisease:D010661 denotes phenylketonuria
T2 119-134 SpecificDisease:D010661 denotes Phenylketonuria
T3 136-139 SpecificDisease:D010661 denotes PKU
T4 147-174 DiseaseClass:D030342 denotes autosomal recessive disease
T5 182-239 SpecificDisease:OMIM:261600 denotes deficiency of a hepatic enzyme, phenylalanine hydroxylase
T6 294-297 SpecificDisease:D010661 denotes PKU
T7 888-891 Modifier:D010661 denotes PKU