Source:http://linkedlifedata.com/resource/lhgdn/association:46941
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:46941 | lhgdn:found_in | pubmed-article:15842381 | lld:lhgdn |
| lhgdn:association:46941 | lhgdn:geneRifSource | analysis of missense mutations in two patients with factor XI deficiency (Val271Leu and Tyr351Ser) and one patient with combined factor XI and factor IX deficiency (Phe349Val) [letter] | lld:lhgdn |
| lhgdn:association:46941 | lhgdn:mesh_code | D002836 | lld:lhgdn |
| lhgdn:association:46941 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
| lhgdn:association:46941 | lhgdn:umls_code | umls-concept:C0008533 | lld:mappings |
| entrez-gene:2158 | lhgdn:associationId | lhgdn:association:46941 | lld:lhgdn |