Source:http://linkedlifedata.com/resource/lhgdn/association:10577
Subject | Predicate | Object | Context |
---|---|---|---|
lhgdn:association:10577 | lhgdn:found_in | pubmed-article:18413478 | lld:lhgdn |
lhgdn:association:10577 | lhgdn:geneRifSource | To identify early abnormalities of ocular motor function in individuals who have the spinocerebellar ataxia type 6 (SCA6) gene (CACNA1A) but no clinical symptoms. | lld:lhgdn |
lhgdn:association:10577 | lhgdn:mesh_code | D020754 | lld:lhgdn |
lhgdn:association:10577 | lhgdn:associationIdType | http://bio2rdf.org/euadr:Po... | lld:lhgdn |
lhgdn:association:10577 | lhgdn:umls_code | umls-concept:C0752125 | lld:mappings |
entrez-gene:773 | lhgdn:associationId | lhgdn:association:10577 | lld:lhgdn |