Source:http://linkedlifedata.com/resource/lhgdn/association:10548
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:10548 | lhgdn:found_in | pubmed-article:18279427 | lld:lhgdn |
| lhgdn:association:10548 | lhgdn:geneRifSource | T666M CACNA1A mutation in early onset familial hemiplegic migraine type 1 with cerebellar atrophy and mental retardation | lld:lhgdn |
| lhgdn:association:10548 | lhgdn:mesh_code | D020325 | lld:lhgdn |
| lhgdn:association:10548 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
| lhgdn:association:10548 | lhgdn:umls_code | umls-concept:C1735856 | lld:mappings |
| entrez-gene:773 | lhgdn:associationId | lhgdn:association:10548 | lld:lhgdn |