Source:http://linkedlifedata.com/resource/lhgdn/association:28775
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:28775 | lhgdn:found_in | pubmed-article:17357132 | lld:lhgdn |
| lhgdn:association:28775 | lhgdn:geneRifSource | among 686 autosomal dominant spinocerebellar ataxia families in our cohort, 57 families were identified to have 65 affected individuals, who carried the C-to-T substitution of the puratrophin-1 gene | lld:lhgdn |
| lhgdn:association:28775 | lhgdn:mesh_code | D020754 | lld:lhgdn |
| lhgdn:association:28775 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
| lhgdn:association:28775 | lhgdn:umls_code | umls-concept:C0752125 | lld:mappings |
| entrez-gene:25894 | lhgdn:associationId | lhgdn:association:28775 | lld:lhgdn |