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PubMed:23174215 JSONTXT 12 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
T1 145-188 disease:C0342642 denotes Autosomal dominant hypophosphatemic rickets
T5 145-188 disease:C0342642 denotes Autosomal dominant hypophosphatemic rickets
T3 190-194 disease:C0342642 denotes ADHR
T7 190-194 disease:C0342642 denotes ADHR
T9 206-222 disease:C0019247 denotes genetic disorder
T11 291-303 disease:C0029442 denotes osteomalacia
T0 392-419 gene:8074 denotes fibroblast growth factor 23
T2 392-419 gene:8074 denotes fibroblast growth factor 23
T4 421-426 gene:8074 denotes FGF23
T6 421-426 gene:8074 denotes FGF23
T8 421-426 gene:8074 denotes FGF23
T10 421-426 gene:8074 denotes FGF23
R1 T0 T1 associated_with fibroblast growth factor 23,Autosomal dominant hypophosphatemic rickets
R2 T2 T3 associated_with fibroblast growth factor 23,ADHR
R3 T4 T5 associated_with FGF23,Autosomal dominant hypophosphatemic rickets
R4 T6 T7 associated_with FGF23,ADHR
R5 T8 T9 associated_with FGF23,genetic disorder
R6 T10 T11 associated_with FGF23,osteomalacia