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PubMed:10400640 / 250-293 JSONTXT

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PubmedHPO

Id Subject Object Predicate Lexical cue
T1 0-8 HP_0001417 denotes X-linked
T2 27-43 HP_0003202 denotes muscular atrophy

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10400640-1#116#159#diseaseC1839259 0-43 diseaseC1839259 denotes X-linked spinal and bulbar muscular atrophy
10400640-1#116#159#diseaseC1839259 0-43 diseaseC1839259 denotes X-linked spinal and bulbar muscular atrophy

DisGeNET

Id Subject Object Predicate Lexical cue
T1 0-43 disease:C1839259 denotes X-linked spinal and bulbar muscular atrophy
T3 0-43 disease:C1839259 denotes X-linked spinal and bulbar muscular atrophy

GlyCosmos15-HP

Id Subject Object Predicate Lexical cue hp_id
T1 27-43 Phenotype denotes muscular atrophy HP:0003202

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T2 9-43 Disease denotes spinal and bulbar muscular atrophy http://purl.obolibrary.org/obo/MONDO_0010735

Anatomy-UBERON

Id Subject Object Predicate Lexical cue uberon_id
T2 20-26 Body_part denotes bulbar http://purl.obolibrary.org/obo/UBERON_0022272