Source:http://linkedlifedata.com/resource/lhgdn/association:27783
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:27783 | lhgdn:found_in | pubmed-article:15159495 | lld:lhgdn |
| lhgdn:association:27783 | lhgdn:geneRifSource | 3 putative A1A2 mutations (D718N, R763H, P979L) & 3 that await validation (P796R, E902K, X1021R) were found in familial hemiplegic migraine/and P979L may predispose to seizures and mental retardation/does not play a major role in sporadic HM. | lld:lhgdn |
| lhgdn:association:27783 | lhgdn:mesh_code | D012640 | lld:lhgdn |
| lhgdn:association:27783 | lhgdn:associationIdType | http://bio2rdf.org/euadr:Po... | lld:lhgdn |
| lhgdn:association:27783 | lhgdn:umls_code | umls-concept:C0751494 | lld:mappings |
| entrez-gene:477 | lhgdn:associationId | lhgdn:association:27783 | lld:lhgdn |