Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP507338.RA6tioFkJQ2Q13YZot1RDeGWOzXWYQ8fmfX79NFXq0VPc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP507338.RA6tioFkJQ2Q13YZot1RDeGWOzXWYQ8fmfX79NFXq0VPc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP507338.RA6tioFkJQ2Q13YZot1RDeGWOzXWYQ8fmfX79NFXq0VPc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP507338.RA6tioFkJQ2Q13YZot1RDeGWOzXWYQ8fmfX79NFXq0VPc130_provenance.
- NP507338.RA6tioFkJQ2Q13YZot1RDeGWOzXWYQ8fmfX79NFXq0VPc130_assertion description "[After adjustment for multiple testing, we found a strong association between CLL risk and six genetic variants: CCNH (rs2266690, V270A), APAF1 (rs17028658, 3'region), IL16 (rs4505265, first intron), CASP8 (rs1045485, D302H), NOS2A (rs2779251, promoter), and CCR7 (rs3136687, intron 1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP507338.RA6tioFkJQ2Q13YZot1RDeGWOzXWYQ8fmfX79NFXq0VPc130_provenance.
- NP507338.RA6tioFkJQ2Q13YZot1RDeGWOzXWYQ8fmfX79NFXq0VPc130_assertion evidence source_evidence_literature NP507338.RA6tioFkJQ2Q13YZot1RDeGWOzXWYQ8fmfX79NFXq0VPc130_provenance.
- NP507338.RA6tioFkJQ2Q13YZot1RDeGWOzXWYQ8fmfX79NFXq0VPc130_assertion SIO_000772 19074885 NP507338.RA6tioFkJQ2Q13YZot1RDeGWOzXWYQ8fmfX79NFXq0VPc130_provenance.
- NP507338.RA6tioFkJQ2Q13YZot1RDeGWOzXWYQ8fmfX79NFXq0VPc130_assertion wasDerivedFrom befree-20150227 NP507338.RA6tioFkJQ2Q13YZot1RDeGWOzXWYQ8fmfX79NFXq0VPc130_provenance.
- NP507338.RA6tioFkJQ2Q13YZot1RDeGWOzXWYQ8fmfX79NFXq0VPc130_assertion wasGeneratedBy ECO_0000203 NP507338.RA6tioFkJQ2Q13YZot1RDeGWOzXWYQ8fmfX79NFXq0VPc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP507338.RA6tioFkJQ2Q13YZot1RDeGWOzXWYQ8fmfX79NFXq0VPc130_provenance.