| Subject | Predicate | Object | Context |
|---|---|---|---|
| gene-rif:411805 | rdf:type | entrezgene:GeneRif | lld:entrezgene |
| gene-rif:411805 | entrezgene:geneRifText | A family having type 2B von Willebrand disease with an RW1306W mutation is described. Severe thrombocytopenia leads to normalization of high molecular weight multimers. | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:geneRif | gene-rif:411805 | lld:entrezgene |