Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP549277.RA_vjOiH6UUUIj0oWgfo9sa206MZ_V51H91BwcYKZoKEM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP549277.RA_vjOiH6UUUIj0oWgfo9sa206MZ_V51H91BwcYKZoKEM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP549277.RA_vjOiH6UUUIj0oWgfo9sa206MZ_V51H91BwcYKZoKEM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP549277.RA_vjOiH6UUUIj0oWgfo9sa206MZ_V51H91BwcYKZoKEM130_provenance.
- NP549277.RA_vjOiH6UUUIj0oWgfo9sa206MZ_V51H91BwcYKZoKEM130_assertion description "[von Willebrand disease (VWD) type 3 is characterized by extremely low levels of von Willebrand factor (VWF) in plasma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP549277.RA_vjOiH6UUUIj0oWgfo9sa206MZ_V51H91BwcYKZoKEM130_provenance.
- NP549277.RA_vjOiH6UUUIj0oWgfo9sa206MZ_V51H91BwcYKZoKEM130_assertion evidence source_evidence_literature NP549277.RA_vjOiH6UUUIj0oWgfo9sa206MZ_V51H91BwcYKZoKEM130_provenance.
- NP549277.RA_vjOiH6UUUIj0oWgfo9sa206MZ_V51H91BwcYKZoKEM130_assertion SIO_000772 16690331 NP549277.RA_vjOiH6UUUIj0oWgfo9sa206MZ_V51H91BwcYKZoKEM130_provenance.
- NP549277.RA_vjOiH6UUUIj0oWgfo9sa206MZ_V51H91BwcYKZoKEM130_assertion wasDerivedFrom befree-2016 NP549277.RA_vjOiH6UUUIj0oWgfo9sa206MZ_V51H91BwcYKZoKEM130_provenance.
- NP549277.RA_vjOiH6UUUIj0oWgfo9sa206MZ_V51H91BwcYKZoKEM130_assertion wasGeneratedBy ECO_0000203 NP549277.RA_vjOiH6UUUIj0oWgfo9sa206MZ_V51H91BwcYKZoKEM130_provenance.
- befree-2016 importedOn "2016-02-19" NP549277.RA_vjOiH6UUUIj0oWgfo9sa206MZ_V51H91BwcYKZoKEM130_provenance.