Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP569464.RAqfiXZPmxXMOXsWyXs5_zVFerWBqfBrcWvgITww8wBpU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP569464.RAqfiXZPmxXMOXsWyXs5_zVFerWBqfBrcWvgITww8wBpU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP569464.RAqfiXZPmxXMOXsWyXs5_zVFerWBqfBrcWvgITww8wBpU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP569464.RAqfiXZPmxXMOXsWyXs5_zVFerWBqfBrcWvgITww8wBpU130_provenance.
- NP569464.RAqfiXZPmxXMOXsWyXs5_zVFerWBqfBrcWvgITww8wBpU130_assertion description "[von Willebrand disease (VWD) is the most frequent inherited disorder of hemostasis and is due to quantitative (types 1 and 3) or qualitative (type 2) defects of von Willebrand factor (VWF).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569464.RAqfiXZPmxXMOXsWyXs5_zVFerWBqfBrcWvgITww8wBpU130_provenance.
- NP569464.RAqfiXZPmxXMOXsWyXs5_zVFerWBqfBrcWvgITww8wBpU130_assertion evidence source_evidence_literature NP569464.RAqfiXZPmxXMOXsWyXs5_zVFerWBqfBrcWvgITww8wBpU130_provenance.
- NP569464.RAqfiXZPmxXMOXsWyXs5_zVFerWBqfBrcWvgITww8wBpU130_assertion SIO_000772 16977566 NP569464.RAqfiXZPmxXMOXsWyXs5_zVFerWBqfBrcWvgITww8wBpU130_provenance.
- NP569464.RAqfiXZPmxXMOXsWyXs5_zVFerWBqfBrcWvgITww8wBpU130_assertion wasDerivedFrom befree-2016 NP569464.RAqfiXZPmxXMOXsWyXs5_zVFerWBqfBrcWvgITww8wBpU130_provenance.
- NP569464.RAqfiXZPmxXMOXsWyXs5_zVFerWBqfBrcWvgITww8wBpU130_assertion wasGeneratedBy ECO_0000203 NP569464.RAqfiXZPmxXMOXsWyXs5_zVFerWBqfBrcWvgITww8wBpU130_provenance.
- befree-2016 importedOn "2016-02-19" NP569464.RAqfiXZPmxXMOXsWyXs5_zVFerWBqfBrcWvgITww8wBpU130_provenance.