Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP776063.RA5YQUgL6C2aIujXDFBQfVZUGJK0nQIxzPtcZ9v3NEQbg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP776063.RA5YQUgL6C2aIujXDFBQfVZUGJK0nQIxzPtcZ9v3NEQbg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP776063.RA5YQUgL6C2aIujXDFBQfVZUGJK0nQIxzPtcZ9v3NEQbg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP776063.RA5YQUgL6C2aIujXDFBQfVZUGJK0nQIxzPtcZ9v3NEQbg130_provenance.
- NP776063.RA5YQUgL6C2aIujXDFBQfVZUGJK0nQIxzPtcZ9v3NEQbg130_assertion description "[Decreased von Willebrand factor (VWF)-cleaving protease activity (<5%) has been implicated in patients with congenital thrombotic thrombocytopenic purpura-hemolytic uremic syndrome (Upshaw-Schulman syndrome) and associated with mutations within the ADAMTS13 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776063.RA5YQUgL6C2aIujXDFBQfVZUGJK0nQIxzPtcZ9v3NEQbg130_provenance.
- NP776063.RA5YQUgL6C2aIujXDFBQfVZUGJK0nQIxzPtcZ9v3NEQbg130_assertion evidence source_evidence_literature NP776063.RA5YQUgL6C2aIujXDFBQfVZUGJK0nQIxzPtcZ9v3NEQbg130_provenance.
- NP776063.RA5YQUgL6C2aIujXDFBQfVZUGJK0nQIxzPtcZ9v3NEQbg130_assertion SIO_000772 15551280 NP776063.RA5YQUgL6C2aIujXDFBQfVZUGJK0nQIxzPtcZ9v3NEQbg130_provenance.
- NP776063.RA5YQUgL6C2aIujXDFBQfVZUGJK0nQIxzPtcZ9v3NEQbg130_assertion wasDerivedFrom befree-20150227 NP776063.RA5YQUgL6C2aIujXDFBQfVZUGJK0nQIxzPtcZ9v3NEQbg130_provenance.
- NP776063.RA5YQUgL6C2aIujXDFBQfVZUGJK0nQIxzPtcZ9v3NEQbg130_assertion wasGeneratedBy ECO_0000203 NP776063.RA5YQUgL6C2aIujXDFBQfVZUGJK0nQIxzPtcZ9v3NEQbg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP776063.RA5YQUgL6C2aIujXDFBQfVZUGJK0nQIxzPtcZ9v3NEQbg130_provenance.