Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP303297.RA1XP0mXHGFfNgfmuutHBVMDCIjoqC4dDukFivRssevNs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP303297.RA1XP0mXHGFfNgfmuutHBVMDCIjoqC4dDukFivRssevNs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP303297.RA1XP0mXHGFfNgfmuutHBVMDCIjoqC4dDukFivRssevNs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP303297.RA1XP0mXHGFfNgfmuutHBVMDCIjoqC4dDukFivRssevNs130_provenance.
- NP303297.RA1XP0mXHGFfNgfmuutHBVMDCIjoqC4dDukFivRssevNs130_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." NP303297.RA1XP0mXHGFfNgfmuutHBVMDCIjoqC4dDukFivRssevNs130_provenance.
- NP303297.RA1XP0mXHGFfNgfmuutHBVMDCIjoqC4dDukFivRssevNs130_assertion evidence source_evidence_literature NP303297.RA1XP0mXHGFfNgfmuutHBVMDCIjoqC4dDukFivRssevNs130_provenance.
- NP303297.RA1XP0mXHGFfNgfmuutHBVMDCIjoqC4dDukFivRssevNs130_assertion SIO_000772 19563498 NP303297.RA1XP0mXHGFfNgfmuutHBVMDCIjoqC4dDukFivRssevNs130_provenance.
- NP303297.RA1XP0mXHGFfNgfmuutHBVMDCIjoqC4dDukFivRssevNs130_assertion wasDerivedFrom befree-20140225 NP303297.RA1XP0mXHGFfNgfmuutHBVMDCIjoqC4dDukFivRssevNs130_provenance.
- NP303297.RA1XP0mXHGFfNgfmuutHBVMDCIjoqC4dDukFivRssevNs130_assertion wasGeneratedBy ECO_0000203 NP303297.RA1XP0mXHGFfNgfmuutHBVMDCIjoqC4dDukFivRssevNs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP303297.RA1XP0mXHGFfNgfmuutHBVMDCIjoqC4dDukFivRssevNs130_provenance.