Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP492958.RAYYwq8uw1aj8hTjOvFNP8hk2WA_y0SqdrmBqb1ztFCHY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP492958.RAYYwq8uw1aj8hTjOvFNP8hk2WA_y0SqdrmBqb1ztFCHY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP492958.RAYYwq8uw1aj8hTjOvFNP8hk2WA_y0SqdrmBqb1ztFCHY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP492958.RAYYwq8uw1aj8hTjOvFNP8hk2WA_y0SqdrmBqb1ztFCHY130_provenance.
- NP492958.RAYYwq8uw1aj8hTjOvFNP8hk2WA_y0SqdrmBqb1ztFCHY130_assertion description "[Functional deficiency or absence of the human von Willebrand factor (VWF)-cleaving protease (VWF-cp), recently termed ADAMTS13, has been shown to cause acquired and congenital thrombotic thrombocytopenic purpura (TTP), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP492958.RAYYwq8uw1aj8hTjOvFNP8hk2WA_y0SqdrmBqb1ztFCHY130_provenance.
- NP492958.RAYYwq8uw1aj8hTjOvFNP8hk2WA_y0SqdrmBqb1ztFCHY130_assertion evidence source_evidence_literature NP492958.RAYYwq8uw1aj8hTjOvFNP8hk2WA_y0SqdrmBqb1ztFCHY130_provenance.
- NP492958.RAYYwq8uw1aj8hTjOvFNP8hk2WA_y0SqdrmBqb1ztFCHY130_assertion SIO_000772 15869605 NP492958.RAYYwq8uw1aj8hTjOvFNP8hk2WA_y0SqdrmBqb1ztFCHY130_provenance.
- NP492958.RAYYwq8uw1aj8hTjOvFNP8hk2WA_y0SqdrmBqb1ztFCHY130_assertion wasDerivedFrom befree-2016 NP492958.RAYYwq8uw1aj8hTjOvFNP8hk2WA_y0SqdrmBqb1ztFCHY130_provenance.
- NP492958.RAYYwq8uw1aj8hTjOvFNP8hk2WA_y0SqdrmBqb1ztFCHY130_assertion wasGeneratedBy ECO_0000203 NP492958.RAYYwq8uw1aj8hTjOvFNP8hk2WA_y0SqdrmBqb1ztFCHY130_provenance.
- befree-2016 importedOn "2016-02-19" NP492958.RAYYwq8uw1aj8hTjOvFNP8hk2WA_y0SqdrmBqb1ztFCHY130_provenance.