Source:http://linkedlifedata.com/resource/lhgdn/association:40024
Subject | Predicate | Object | Context |
---|---|---|---|
lhgdn:association:40024 | lhgdn:found_in | pubmed-article:16211615 | lld:lhgdn |
lhgdn:association:40024 | lhgdn:geneRifSource | a distinct SCA (spinocerebellar ataxia) phenotype (SCA27) is associated with a F145S mutation in the fibroblast growth factor 14 (FGF14) gene on chromosome 13q34. | lld:lhgdn |
lhgdn:association:40024 | lhgdn:mesh_code | D020754 | lld:lhgdn |
lhgdn:association:40024 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
lhgdn:association:40024 | lhgdn:umls_code | umls-concept:C0752125 | lld:mappings |
entrez-gene:2259 | lhgdn:associationId | lhgdn:association:40024 | lld:lhgdn |