Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP768300.RAv9P1mTee4MPLFxtqPewUkTWrNhVU3n0P3KyzfoiBIzY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP768300.RAv9P1mTee4MPLFxtqPewUkTWrNhVU3n0P3KyzfoiBIzY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768300.RAv9P1mTee4MPLFxtqPewUkTWrNhVU3n0P3KyzfoiBIzY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768300.RAv9P1mTee4MPLFxtqPewUkTWrNhVU3n0P3KyzfoiBIzY130_provenance.
- NP768300.RAv9P1mTee4MPLFxtqPewUkTWrNhVU3n0P3KyzfoiBIzY130_assertion description "[Hypermethylation at APC (3.0 vs 6.7%), CDH1 (15.6 vs 0%), GSTP1 (21.9 vs 6.7%) and TIMP3 (6.3 vs 0%) was infrequent in pRCC and normal tissue.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768300.RAv9P1mTee4MPLFxtqPewUkTWrNhVU3n0P3KyzfoiBIzY130_provenance.
- NP768300.RAv9P1mTee4MPLFxtqPewUkTWrNhVU3n0P3KyzfoiBIzY130_assertion evidence source_evidence_literature NP768300.RAv9P1mTee4MPLFxtqPewUkTWrNhVU3n0P3KyzfoiBIzY130_provenance.
- NP768300.RAv9P1mTee4MPLFxtqPewUkTWrNhVU3n0P3KyzfoiBIzY130_assertion SIO_000772 20553257 NP768300.RAv9P1mTee4MPLFxtqPewUkTWrNhVU3n0P3KyzfoiBIzY130_provenance.
- NP768300.RAv9P1mTee4MPLFxtqPewUkTWrNhVU3n0P3KyzfoiBIzY130_assertion wasDerivedFrom befree-20140225 NP768300.RAv9P1mTee4MPLFxtqPewUkTWrNhVU3n0P3KyzfoiBIzY130_provenance.
- NP768300.RAv9P1mTee4MPLFxtqPewUkTWrNhVU3n0P3KyzfoiBIzY130_assertion wasGeneratedBy ECO_0000203 NP768300.RAv9P1mTee4MPLFxtqPewUkTWrNhVU3n0P3KyzfoiBIzY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP768300.RAv9P1mTee4MPLFxtqPewUkTWrNhVU3n0P3KyzfoiBIzY130_provenance.