Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP303297.RA1XP0mXHGFfNgfmuutHBVMDCIjoqC4dDukFivRssevNs130_assertion> ?p ?o ?g. }
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- NP303297.RA1XP0mXHGFfNgfmuutHBVMDCIjoqC4dDukFivRssevNs130_assertion type Assertion NP303297.RA1XP0mXHGFfNgfmuutHBVMDCIjoqC4dDukFivRssevNs130_head.
- 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.