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PubMed:2303461 / 96-232 JSONTXT

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sentences

Id Subject Object Predicate Lexical cue
T2 0-136 Sentence denotes Congenital adrenal hyperplasia (CAH) is a common recessive genetic disease caused mainly by steroid 21-hydroxylase (P450c21) deficiency.
T2 0-136 Sentence denotes Congenital adrenal hyperplasia (CAH) is a common recessive genetic disease caused mainly by steroid 21-hydroxylase (P450c21) deficiency.

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 0-30 HP_0008258 denotes Congenital adrenal hyperplasia
T2 11-30 HP_0008221 denotes adrenal hyperplasia

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
2303461-1#92#114#gene1589 92-114 gene1589 denotes steroid 21-hydroxylase
2303461-1#116#123#gene1589 116-123 gene1589 denotes P450c21
2303461-1#0#30#diseaseC0001627 0-30 diseaseC0001627 denotes Congenital adrenal hyperplasia
92#114#gene15890#30#diseaseC0001627 2303461-1#92#114#gene1589 2303461-1#0#30#diseaseC0001627 associated_with steroid 21-hydroxylase,Congenital adrenal hyperplasia
116#123#gene15890#30#diseaseC0001627 2303461-1#116#123#gene1589 2303461-1#0#30#diseaseC0001627 associated_with P450c21,Congenital adrenal hyperplasia

PubCasesHPO

Id Subject Object Predicate Lexical cue
AB1 0-30 HP:0008258 denotes Congenital adrenal hyperplasia

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T2 0-30 Disease denotes Congenital adrenal hyperplasia http://purl.obolibrary.org/obo/MONDO_0015898
T3 11-30 Disease denotes adrenal hyperplasia http://purl.obolibrary.org/obo/MONDO_0018479
T4 32-35 Disease denotes CAH http://purl.obolibrary.org/obo/MONDO_0018479|http://purl.obolibrary.org/obo/MONDO_0015898
T6 59-74 Disease denotes genetic disease http://purl.obolibrary.org/obo/MONDO_0003847

Anatomy-UBERON

Id Subject Object Predicate Lexical cue uberon_id
T1 11-18 Body_part denotes adrenal http://purl.obolibrary.org/obo/UBERON_0002369

HP-phenotype

Id Subject Object Predicate Lexical cue hp_id
T1 0-30 Phenotype denotes Congenital adrenal hyperplasia HP:0008258
T2 32-35 Phenotype denotes CAH HP:0008258