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PubMed:18655527 JSONTXT

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DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
18655527-1#44#49#gene1589 221-226 gene1589 denotes CYP21
18655527-1#17#42#diseaseC2936858 194-219 diseaseC2936858 denotes 21-hydroxylase deficiency
18655527-1#53#83#diseaseC0001627 230-260 diseaseC0001627 denotes congenital adrenal hyperplasia
44#49#gene158917#42#diseaseC2936858 18655527-1#44#49#gene1589 18655527-1#17#42#diseaseC2936858 associated_with CYP21,21-hydroxylase deficiency
44#49#gene158953#83#diseaseC0001627 18655527-1#44#49#gene1589 18655527-1#53#83#diseaseC0001627 associated_with CYP21,congenital adrenal hyperplasia