Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP377524.RAB5K22-vAb3z390bGSVK8kh58VjpffOeH2jz7CCJAp4U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP377524.RAB5K22-vAb3z390bGSVK8kh58VjpffOeH2jz7CCJAp4U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP377524.RAB5K22-vAb3z390bGSVK8kh58VjpffOeH2jz7CCJAp4U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP377524.RAB5K22-vAb3z390bGSVK8kh58VjpffOeH2jz7CCJAp4U130_provenance.
- NP377524.RAB5K22-vAb3z390bGSVK8kh58VjpffOeH2jz7CCJAp4U130_assertion description "[There is sufficient epidemiological evidence suggesting a link between genetic polymorphism and haplotypes of microsomal epoxide hydrolase (mEPHX) and X-ray cross-complementing group 1 (XRCC1) with altered cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP377524.RAB5K22-vAb3z390bGSVK8kh58VjpffOeH2jz7CCJAp4U130_provenance.
- NP377524.RAB5K22-vAb3z390bGSVK8kh58VjpffOeH2jz7CCJAp4U130_assertion evidence source_evidence_literature NP377524.RAB5K22-vAb3z390bGSVK8kh58VjpffOeH2jz7CCJAp4U130_provenance.
- NP377524.RAB5K22-vAb3z390bGSVK8kh58VjpffOeH2jz7CCJAp4U130_assertion SIO_000772 19754350 NP377524.RAB5K22-vAb3z390bGSVK8kh58VjpffOeH2jz7CCJAp4U130_provenance.
- NP377524.RAB5K22-vAb3z390bGSVK8kh58VjpffOeH2jz7CCJAp4U130_assertion wasDerivedFrom befree-20150227 NP377524.RAB5K22-vAb3z390bGSVK8kh58VjpffOeH2jz7CCJAp4U130_provenance.
- NP377524.RAB5K22-vAb3z390bGSVK8kh58VjpffOeH2jz7CCJAp4U130_assertion wasGeneratedBy ECO_0000203 NP377524.RAB5K22-vAb3z390bGSVK8kh58VjpffOeH2jz7CCJAp4U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP377524.RAB5K22-vAb3z390bGSVK8kh58VjpffOeH2jz7CCJAp4U130_provenance.