Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP323280.RANQnd_--DjnqiMcvNfb4NRJC4lLdoTrFi7h5fOMUepvY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP323280.RANQnd_--DjnqiMcvNfb4NRJC4lLdoTrFi7h5fOMUepvY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP323280.RANQnd_--DjnqiMcvNfb4NRJC4lLdoTrFi7h5fOMUepvY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP323280.RANQnd_--DjnqiMcvNfb4NRJC4lLdoTrFi7h5fOMUepvY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP323280.RANQnd_--DjnqiMcvNfb4NRJC4lLdoTrFi7h5fOMUepvY130_provenance.
- NP323280.RANQnd_--DjnqiMcvNfb4NRJC4lLdoTrFi7h5fOMUepvY130_assertion wasGeneratedBy ECO_0000203 NP323280.RANQnd_--DjnqiMcvNfb4NRJC4lLdoTrFi7h5fOMUepvY130_provenance.
- NP323280.RANQnd_--DjnqiMcvNfb4NRJC4lLdoTrFi7h5fOMUepvY130_assertion wasDerivedFrom befree-20150227 NP323280.RANQnd_--DjnqiMcvNfb4NRJC4lLdoTrFi7h5fOMUepvY130_provenance.
- NP323280.RANQnd_--DjnqiMcvNfb4NRJC4lLdoTrFi7h5fOMUepvY130_assertion SIO_000772 9684781 NP323280.RANQnd_--DjnqiMcvNfb4NRJC4lLdoTrFi7h5fOMUepvY130_provenance.
- NP323280.RANQnd_--DjnqiMcvNfb4NRJC4lLdoTrFi7h5fOMUepvY130_assertion evidence source_evidence_literature NP323280.RANQnd_--DjnqiMcvNfb4NRJC4lLdoTrFi7h5fOMUepvY130_provenance.
- NP323280.RANQnd_--DjnqiMcvNfb4NRJC4lLdoTrFi7h5fOMUepvY130_assertion description "[The majority of patients with type 2N von Willebrand disease (VWD type 2N) have mutations in the region of the von Willebrand factor (VWF) gene encoding the factor VIII binding domain of VWF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323280.RANQnd_--DjnqiMcvNfb4NRJC4lLdoTrFi7h5fOMUepvY130_provenance.