Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP52796.RARr8H1v56i1OxhjrmFL4x3y2vQ4BHcI5gIehQhvqN0UU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP52796.RARr8H1v56i1OxhjrmFL4x3y2vQ4BHcI5gIehQhvqN0UU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP52796.RARr8H1v56i1OxhjrmFL4x3y2vQ4BHcI5gIehQhvqN0UU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP52796.RARr8H1v56i1OxhjrmFL4x3y2vQ4BHcI5gIehQhvqN0UU130_provenance.
- NP52796.RARr8H1v56i1OxhjrmFL4x3y2vQ4BHcI5gIehQhvqN0UU130_assertion description "[The frequency of either the FVL or prothrombin sequence variant was not increased in idiopathic PE patients compared with nonidiopathic PE patients or patients who had PE excluded.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52796.RARr8H1v56i1OxhjrmFL4x3y2vQ4BHcI5gIehQhvqN0UU130_provenance.
- NP52796.RARr8H1v56i1OxhjrmFL4x3y2vQ4BHcI5gIehQhvqN0UU130_assertion evidence source_evidence_literature NP52796.RARr8H1v56i1OxhjrmFL4x3y2vQ4BHcI5gIehQhvqN0UU130_provenance.
- NP52796.RARr8H1v56i1OxhjrmFL4x3y2vQ4BHcI5gIehQhvqN0UU130_assertion SIO_000772 16574759 NP52796.RARr8H1v56i1OxhjrmFL4x3y2vQ4BHcI5gIehQhvqN0UU130_provenance.
- NP52796.RARr8H1v56i1OxhjrmFL4x3y2vQ4BHcI5gIehQhvqN0UU130_assertion wasDerivedFrom gad-20150221 NP52796.RARr8H1v56i1OxhjrmFL4x3y2vQ4BHcI5gIehQhvqN0UU130_provenance.
- NP52796.RARr8H1v56i1OxhjrmFL4x3y2vQ4BHcI5gIehQhvqN0UU130_assertion wasGeneratedBy ECO_0000203 NP52796.RARr8H1v56i1OxhjrmFL4x3y2vQ4BHcI5gIehQhvqN0UU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP52796.RARr8H1v56i1OxhjrmFL4x3y2vQ4BHcI5gIehQhvqN0UU130_provenance.