Source:http://linkedlifedata.com/resource/lhgdn/association:21463
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:21463 | lhgdn:found_in | pubmed-article:18505993 | lld:lhgdn |
| lhgdn:association:21463 | lhgdn:geneRifSource | Nine percent of consecutive juvenile myoclonic epilepsy cases from Mexico and Honduras clinics and 3% of clinic patients from Japan carry mutations in Myoclonin1/EFCH1 | lld:lhgdn |
| lhgdn:association:21463 | lhgdn:mesh_code | D020190 | lld:lhgdn |
| lhgdn:association:21463 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
| lhgdn:association:21463 | lhgdn:umls_code | umls-concept:C0270853 | lld:mappings |
| entrez-gene:114327 | lhgdn:associationId | lhgdn:association:21463 | lld:lhgdn |