Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP155222.RACpdBHUNfg3Z6o8hhh3s_5H9iVsWbx0OzGcvkCdBQBzE130_assertion> ?p ?o ?g. }
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- NP155222.RACpdBHUNfg3Z6o8hhh3s_5H9iVsWbx0OzGcvkCdBQBzE130_assertion type Assertion NP155222.RACpdBHUNfg3Z6o8hhh3s_5H9iVsWbx0OzGcvkCdBQBzE130_head.
- NP155222.RACpdBHUNfg3Z6o8hhh3s_5H9iVsWbx0OzGcvkCdBQBzE130_assertion description "[As PT-VWD shares most of the clinical and laboratory features of subtype 2B VWD, the differential diagnosis between these two inherited bleeding disorders requires either platelet-mixing or molecular genetic studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP155222.RACpdBHUNfg3Z6o8hhh3s_5H9iVsWbx0OzGcvkCdBQBzE130_provenance.
- NP155222.RACpdBHUNfg3Z6o8hhh3s_5H9iVsWbx0OzGcvkCdBQBzE130_assertion evidence source_evidence_literature NP155222.RACpdBHUNfg3Z6o8hhh3s_5H9iVsWbx0OzGcvkCdBQBzE130_provenance.
- NP155222.RACpdBHUNfg3Z6o8hhh3s_5H9iVsWbx0OzGcvkCdBQBzE130_assertion SIO_000772 18333841 NP155222.RACpdBHUNfg3Z6o8hhh3s_5H9iVsWbx0OzGcvkCdBQBzE130_provenance.
- NP155222.RACpdBHUNfg3Z6o8hhh3s_5H9iVsWbx0OzGcvkCdBQBzE130_assertion wasDerivedFrom befree-20140225 NP155222.RACpdBHUNfg3Z6o8hhh3s_5H9iVsWbx0OzGcvkCdBQBzE130_provenance.
- NP155222.RACpdBHUNfg3Z6o8hhh3s_5H9iVsWbx0OzGcvkCdBQBzE130_assertion wasGeneratedBy ECO_0000203 NP155222.RACpdBHUNfg3Z6o8hhh3s_5H9iVsWbx0OzGcvkCdBQBzE130_provenance.