Source:http://linkedlifedata.com/resource/lhgdn/association:18735
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:18735 | lhgdn:found_in | pubmed-article:12592226 | lld:lhgdn |
| lhgdn:association:18735 | lhgdn:geneRifSource | Recessive retinitis pigmentosa and Leber congenital amaurosis are rarely if ever associated with changes in the ELOVL4 gene. | lld:lhgdn |
| lhgdn:association:18735 | lhgdn:mesh_code | D001766 | lld:lhgdn |
| lhgdn:association:18735 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
| lhgdn:association:18735 | lhgdn:umls_code | umls-concept:C0456909 | lld:mappings |
| entrez-gene:6785 | lhgdn:associationId | lhgdn:association:18735 | lld:lhgdn |