Source:http://linkedlifedata.com/resource/lhgdn/association:43508
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:43508 | lhgdn:found_in | pubmed-article:16944272 | lld:lhgdn |
| lhgdn:association:43508 | lhgdn:geneRifSource | 169 unrelated individuals suspected of having neurofibromatosis type I (NF1) were referred for NF1 diagnostic testing/disease causing mutations were identified in 109 (64%) cases/comprised 88 sequence alterations, of which 57 were novel. | lld:lhgdn |
| lhgdn:association:43508 | lhgdn:mesh_code | D009456 | lld:lhgdn |
| lhgdn:association:43508 | lhgdn:associationIdType | http://bio2rdf.org/euadr:Ne... | lld:lhgdn |
| lhgdn:association:43508 | lhgdn:umls_code | umls-concept:C0553586 | lld:mappings |
| entrez-gene:4763 | lhgdn:associationId | lhgdn:association:43508 | lld:lhgdn |