Source:http://linkedlifedata.com/resource/lhgdn/association:47476
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:47476 | lhgdn:found_in | pubmed-article:18852482 | lld:lhgdn |
| lhgdn:association:47476 | lhgdn:geneRifSource | study reports a new molecular defect in a family with true prothrombin deficiency; the mother was homozygous for a mutation Arg-Gln in position -39 of the propeptide controlled by exon 1; the son was heterozygosity for the same mutation | lld:lhgdn |
| lhgdn:association:47476 | lhgdn:mesh_code | D007020 | lld:lhgdn |
| lhgdn:association:47476 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
| lhgdn:association:47476 | lhgdn:umls_code | umls-concept:C0020640 | lld:mappings |
| entrez-gene:2147 | lhgdn:associationId | lhgdn:association:47476 | lld:lhgdn |