Source:http://linkedlifedata.com/resource/lhgdn/association:39947
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:39947 | lhgdn:found_in | pubmed-article:19019939 | lld:lhgdn |
| lhgdn:association:39947 | lhgdn:geneRifSource | The pathogenesis of the retinal dots and flecks in Alport syndrome is independent of CFH-dependent mechanisms and, like other clinical features, may depend on the nature of the underlying COL4A5 mutations. | lld:lhgdn |
| lhgdn:association:39947 | lhgdn:mesh_code | D009394 | lld:lhgdn |
| lhgdn:association:39947 | lhgdn:associationIdType | http://bio2rdf.org/euadr:Ne... | lld:lhgdn |
| lhgdn:association:39947 | lhgdn:umls_code | umls-concept:C1567744 | lld:mappings |
| entrez-gene:3075 | lhgdn:associationId | lhgdn:association:39947 | lld:lhgdn |