Source:http://linkedlifedata.com/resource/lhgdn/association:12410
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:12410 | lhgdn:found_in | pubmed-article:18678320 | lld:lhgdn |
| lhgdn:association:12410 | lhgdn:geneRifSource | a mutation in the genomically imprinted potassium channel KCNK9 may have a role in the maternally inherited Birk Barel mental retardation dysmorphism syndrome | lld:lhgdn |
| lhgdn:association:12410 | lhgdn:mesh_code | D008607 | lld:lhgdn |
| lhgdn:association:12410 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
| lhgdn:association:12410 | lhgdn:umls_code | umls-concept:C0917816 | lld:mappings |
| entrez-gene:51305 | lhgdn:associationId | lhgdn:association:12410 | lld:lhgdn |