Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP748076.RARunkSyWz_QGEKlfNcGdsgySLy1dJMq6mu5idvNy6Gi0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP748076.RARunkSyWz_QGEKlfNcGdsgySLy1dJMq6mu5idvNy6Gi0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP748076.RARunkSyWz_QGEKlfNcGdsgySLy1dJMq6mu5idvNy6Gi0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP748076.RARunkSyWz_QGEKlfNcGdsgySLy1dJMq6mu5idvNy6Gi0130_provenance.
- NP748076.RARunkSyWz_QGEKlfNcGdsgySLy1dJMq6mu5idvNy6Gi0130_assertion description "[von Willebrand disease (VWD) type 3 is a rare disorder characterized by absent or <0.1 UmL(-1) of ristocetin cofactor (VWF:RCo), and a very low level of factor VIII (FVIII:C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748076.RARunkSyWz_QGEKlfNcGdsgySLy1dJMq6mu5idvNy6Gi0130_provenance.
- NP748076.RARunkSyWz_QGEKlfNcGdsgySLy1dJMq6mu5idvNy6Gi0130_assertion evidence source_evidence_literature NP748076.RARunkSyWz_QGEKlfNcGdsgySLy1dJMq6mu5idvNy6Gi0130_provenance.
- NP748076.RARunkSyWz_QGEKlfNcGdsgySLy1dJMq6mu5idvNy6Gi0130_assertion SIO_000772 19563498 NP748076.RARunkSyWz_QGEKlfNcGdsgySLy1dJMq6mu5idvNy6Gi0130_provenance.
- NP748076.RARunkSyWz_QGEKlfNcGdsgySLy1dJMq6mu5idvNy6Gi0130_assertion wasDerivedFrom befree-2016 NP748076.RARunkSyWz_QGEKlfNcGdsgySLy1dJMq6mu5idvNy6Gi0130_provenance.
- NP748076.RARunkSyWz_QGEKlfNcGdsgySLy1dJMq6mu5idvNy6Gi0130_assertion wasGeneratedBy ECO_0000203 NP748076.RARunkSyWz_QGEKlfNcGdsgySLy1dJMq6mu5idvNy6Gi0130_provenance.
- befree-2016 importedOn "2016-02-19" NP748076.RARunkSyWz_QGEKlfNcGdsgySLy1dJMq6mu5idvNy6Gi0130_provenance.