Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP541634.RAqwJm8MYUYUmnt2RZDNX8VIi7W6YwjSm_-jJLSo0i9iY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP541634.RAqwJm8MYUYUmnt2RZDNX8VIi7W6YwjSm_-jJLSo0i9iY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP541634.RAqwJm8MYUYUmnt2RZDNX8VIi7W6YwjSm_-jJLSo0i9iY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP541634.RAqwJm8MYUYUmnt2RZDNX8VIi7W6YwjSm_-jJLSo0i9iY130_provenance.
- NP541634.RAqwJm8MYUYUmnt2RZDNX8VIi7W6YwjSm_-jJLSo0i9iY130_assertion description "[We found that the frequency of 939Gln variant at XPC Lys939Gln was significantly lower in PC cases (OR=0.39, P=0.016).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP541634.RAqwJm8MYUYUmnt2RZDNX8VIi7W6YwjSm_-jJLSo0i9iY130_provenance.
- NP541634.RAqwJm8MYUYUmnt2RZDNX8VIi7W6YwjSm_-jJLSo0i9iY130_assertion evidence source_evidence_literature NP541634.RAqwJm8MYUYUmnt2RZDNX8VIi7W6YwjSm_-jJLSo0i9iY130_provenance.
- NP541634.RAqwJm8MYUYUmnt2RZDNX8VIi7W6YwjSm_-jJLSo0i9iY130_assertion SIO_000772 17196815 NP541634.RAqwJm8MYUYUmnt2RZDNX8VIi7W6YwjSm_-jJLSo0i9iY130_provenance.
- NP541634.RAqwJm8MYUYUmnt2RZDNX8VIi7W6YwjSm_-jJLSo0i9iY130_assertion wasDerivedFrom befree-20140225 NP541634.RAqwJm8MYUYUmnt2RZDNX8VIi7W6YwjSm_-jJLSo0i9iY130_provenance.
- NP541634.RAqwJm8MYUYUmnt2RZDNX8VIi7W6YwjSm_-jJLSo0i9iY130_assertion wasGeneratedBy ECO_0000203 NP541634.RAqwJm8MYUYUmnt2RZDNX8VIi7W6YwjSm_-jJLSo0i9iY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP541634.RAqwJm8MYUYUmnt2RZDNX8VIi7W6YwjSm_-jJLSo0i9iY130_provenance.