Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP857233.RAAZ7VV4m2ZAmXIBU9rfYWAFBPBmnu8IiG_o2EqCDmbUk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP857233.RAAZ7VV4m2ZAmXIBU9rfYWAFBPBmnu8IiG_o2EqCDmbUk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP857233.RAAZ7VV4m2ZAmXIBU9rfYWAFBPBmnu8IiG_o2EqCDmbUk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP857233.RAAZ7VV4m2ZAmXIBU9rfYWAFBPBmnu8IiG_o2EqCDmbUk130_provenance.
- NP857233.RAAZ7VV4m2ZAmXIBU9rfYWAFBPBmnu8IiG_o2EqCDmbUk130_assertion description "[The data from this study show overall risk modulation of BCC by variant allele for T241M polymorphism in XRCC3 and gender-specific effect by E185Q polymorphism in NBS1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP857233.RAAZ7VV4m2ZAmXIBU9rfYWAFBPBmnu8IiG_o2EqCDmbUk130_provenance.
- NP857233.RAAZ7VV4m2ZAmXIBU9rfYWAFBPBmnu8IiG_o2EqCDmbUk130_assertion evidence source_evidence_literature NP857233.RAAZ7VV4m2ZAmXIBU9rfYWAFBPBmnu8IiG_o2EqCDmbUk130_provenance.
- NP857233.RAAZ7VV4m2ZAmXIBU9rfYWAFBPBmnu8IiG_o2EqCDmbUk130_assertion SIO_000772 16501254 NP857233.RAAZ7VV4m2ZAmXIBU9rfYWAFBPBmnu8IiG_o2EqCDmbUk130_provenance.
- NP857233.RAAZ7VV4m2ZAmXIBU9rfYWAFBPBmnu8IiG_o2EqCDmbUk130_assertion wasDerivedFrom befree-20140225 NP857233.RAAZ7VV4m2ZAmXIBU9rfYWAFBPBmnu8IiG_o2EqCDmbUk130_provenance.
- NP857233.RAAZ7VV4m2ZAmXIBU9rfYWAFBPBmnu8IiG_o2EqCDmbUk130_assertion wasGeneratedBy ECO_0000203 NP857233.RAAZ7VV4m2ZAmXIBU9rfYWAFBPBmnu8IiG_o2EqCDmbUk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP857233.RAAZ7VV4m2ZAmXIBU9rfYWAFBPBmnu8IiG_o2EqCDmbUk130_provenance.