Source:http://linkedlifedata.com/resource/lhgdn/association:57629
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:57629 | lhgdn:found_in | pubmed-article:15937479 | lld:lhgdn |
| lhgdn:association:57629 | lhgdn:geneRifSource | mutated in generalized epilepsy and paroxysmal dyskinesia and have implications for the pathogenesis of human epilepsy, the neurophysiology of paroxysmal movement disorders and the role of BK channels in neurological disease | lld:lhgdn |
| lhgdn:association:57629 | lhgdn:mesh_code | D002819 | lld:lhgdn |
| lhgdn:association:57629 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
| lhgdn:association:57629 | lhgdn:umls_code | umls-concept:C0699728 | lld:mappings |
| entrez-gene:3778 | lhgdn:associationId | lhgdn:association:57629 | lld:lhgdn |