Source:http://linkedlifedata.com/resource/lhgdn/association:26207
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:26207 | lhgdn:found_in | pubmed-article:12556236 | lld:lhgdn |
| lhgdn:association:26207 | lhgdn:geneRifSource | SMPD1 mutation (r608del) is prevalent among Niemann-Pick disease type b patients from the North-African Maghreb region. | lld:lhgdn |
| lhgdn:association:26207 | lhgdn:mesh_code | D009542 | lld:lhgdn |
| lhgdn:association:26207 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
| lhgdn:association:26207 | lhgdn:umls_code | umls-concept:C0028064 | lld:mappings |
| entrez-gene:6609 | lhgdn:associationId | lhgdn:association:26207 | lld:lhgdn |