Source:http://linkedlifedata.com/resource/lhgdn/association:9240
Subject | Predicate | Object | Context |
---|---|---|---|
lhgdn:association:9240 | lhgdn:found_in | pubmed-article:17846415 | lld:lhgdn |
lhgdn:association:9240 | lhgdn:geneRifSource | Several oculomotor deficits of spinocerebellar ataxia type 17 (SCA17) mutation carriers are compatible with cerebellar degeneration. | lld:lhgdn |
lhgdn:association:9240 | lhgdn:mesh_code | D020754 | lld:lhgdn |
lhgdn:association:9240 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
lhgdn:association:9240 | lhgdn:umls_code | umls-concept:C0752125 | lld:mappings |
entrez-gene:6908 | lhgdn:associationId | lhgdn:association:9240 | lld:lhgdn |