Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP776383.RACpIlA9oPthHYqZknlBHOxpu-WHbThmCtFcVmBkmTxmM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP776383.RACpIlA9oPthHYqZknlBHOxpu-WHbThmCtFcVmBkmTxmM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP776383.RACpIlA9oPthHYqZknlBHOxpu-WHbThmCtFcVmBkmTxmM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP776383.RACpIlA9oPthHYqZknlBHOxpu-WHbThmCtFcVmBkmTxmM130_provenance.
- NP776383.RACpIlA9oPthHYqZknlBHOxpu-WHbThmCtFcVmBkmTxmM130_assertion description "[The defective FVIII carrier function of von Willebrand factor (VWF) identifies type 2N von Willebrand disease (VWD), a variant with a pattern resembling hemophilia A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776383.RACpIlA9oPthHYqZknlBHOxpu-WHbThmCtFcVmBkmTxmM130_provenance.
- NP776383.RACpIlA9oPthHYqZknlBHOxpu-WHbThmCtFcVmBkmTxmM130_assertion evidence source_evidence_literature NP776383.RACpIlA9oPthHYqZknlBHOxpu-WHbThmCtFcVmBkmTxmM130_provenance.
- NP776383.RACpIlA9oPthHYqZknlBHOxpu-WHbThmCtFcVmBkmTxmM130_assertion SIO_000772 17456630 NP776383.RACpIlA9oPthHYqZknlBHOxpu-WHbThmCtFcVmBkmTxmM130_provenance.
- NP776383.RACpIlA9oPthHYqZknlBHOxpu-WHbThmCtFcVmBkmTxmM130_assertion wasDerivedFrom befree-20150227 NP776383.RACpIlA9oPthHYqZknlBHOxpu-WHbThmCtFcVmBkmTxmM130_provenance.
- NP776383.RACpIlA9oPthHYqZknlBHOxpu-WHbThmCtFcVmBkmTxmM130_assertion wasGeneratedBy ECO_0000203 NP776383.RACpIlA9oPthHYqZknlBHOxpu-WHbThmCtFcVmBkmTxmM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP776383.RACpIlA9oPthHYqZknlBHOxpu-WHbThmCtFcVmBkmTxmM130_provenance.