Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP535350.RA-w-WqNquzl7fmkoYqdrIx2lNHzKivRAkLrtwzE6Vz5o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP535350.RA-w-WqNquzl7fmkoYqdrIx2lNHzKivRAkLrtwzE6Vz5o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP535350.RA-w-WqNquzl7fmkoYqdrIx2lNHzKivRAkLrtwzE6Vz5o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP535350.RA-w-WqNquzl7fmkoYqdrIx2lNHzKivRAkLrtwzE6Vz5o130_provenance.
- NP535350.RA-w-WqNquzl7fmkoYqdrIx2lNHzKivRAkLrtwzE6Vz5o130_assertion description "[Carriers of the variant XPD 751Gln allele had an increased risk of low-risk adenomas (OR 1.40, 95% CI 1.03-1.89), while no association was found with risk of carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP535350.RA-w-WqNquzl7fmkoYqdrIx2lNHzKivRAkLrtwzE6Vz5o130_provenance.
- NP535350.RA-w-WqNquzl7fmkoYqdrIx2lNHzKivRAkLrtwzE6Vz5o130_assertion evidence source_evidence_literature NP535350.RA-w-WqNquzl7fmkoYqdrIx2lNHzKivRAkLrtwzE6Vz5o130_provenance.
- NP535350.RA-w-WqNquzl7fmkoYqdrIx2lNHzKivRAkLrtwzE6Vz5o130_assertion SIO_000772 16542436 NP535350.RA-w-WqNquzl7fmkoYqdrIx2lNHzKivRAkLrtwzE6Vz5o130_provenance.
- NP535350.RA-w-WqNquzl7fmkoYqdrIx2lNHzKivRAkLrtwzE6Vz5o130_assertion wasDerivedFrom befree-20140225 NP535350.RA-w-WqNquzl7fmkoYqdrIx2lNHzKivRAkLrtwzE6Vz5o130_provenance.
- NP535350.RA-w-WqNquzl7fmkoYqdrIx2lNHzKivRAkLrtwzE6Vz5o130_assertion wasGeneratedBy ECO_0000203 NP535350.RA-w-WqNquzl7fmkoYqdrIx2lNHzKivRAkLrtwzE6Vz5o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP535350.RA-w-WqNquzl7fmkoYqdrIx2lNHzKivRAkLrtwzE6Vz5o130_provenance.