Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP129709.RA2BWC9JikKt8qaYtysars1aHdV0IoT8bE0PJEITEPRwQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP129709.RA2BWC9JikKt8qaYtysars1aHdV0IoT8bE0PJEITEPRwQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP129709.RA2BWC9JikKt8qaYtysars1aHdV0IoT8bE0PJEITEPRwQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP129709.RA2BWC9JikKt8qaYtysars1aHdV0IoT8bE0PJEITEPRwQ130_provenance.
- NP129709.RA2BWC9JikKt8qaYtysars1aHdV0IoT8bE0PJEITEPRwQ130_assertion description "[Carrying at least one copy of the variant XRCC4 allele (rs1805377) was associated with a significantly increased risk of renal cell carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP129709.RA2BWC9JikKt8qaYtysars1aHdV0IoT8bE0PJEITEPRwQ130_provenance.
- NP129709.RA2BWC9JikKt8qaYtysars1aHdV0IoT8bE0PJEITEPRwQ130_assertion evidence source_evidence_literature NP129709.RA2BWC9JikKt8qaYtysars1aHdV0IoT8bE0PJEITEPRwQ130_provenance.
- NP129709.RA2BWC9JikKt8qaYtysars1aHdV0IoT8bE0PJEITEPRwQ130_assertion SIO_000772 18768505 NP129709.RA2BWC9JikKt8qaYtysars1aHdV0IoT8bE0PJEITEPRwQ130_provenance.
- NP129709.RA2BWC9JikKt8qaYtysars1aHdV0IoT8bE0PJEITEPRwQ130_assertion wasDerivedFrom lhgdn-20090331 NP129709.RA2BWC9JikKt8qaYtysars1aHdV0IoT8bE0PJEITEPRwQ130_provenance.
- NP129709.RA2BWC9JikKt8qaYtysars1aHdV0IoT8bE0PJEITEPRwQ130_assertion wasGeneratedBy ECO_0000203 NP129709.RA2BWC9JikKt8qaYtysars1aHdV0IoT8bE0PJEITEPRwQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP129709.RA2BWC9JikKt8qaYtysars1aHdV0IoT8bE0PJEITEPRwQ130_provenance.