Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP779580.RA_vIXlvgL_XexFiDE3cgEx8TpHogomg0akL-95Lr1Bnw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP779580.RA_vIXlvgL_XexFiDE3cgEx8TpHogomg0akL-95Lr1Bnw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP779580.RA_vIXlvgL_XexFiDE3cgEx8TpHogomg0akL-95Lr1Bnw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP779580.RA_vIXlvgL_XexFiDE3cgEx8TpHogomg0akL-95Lr1Bnw130_provenance.
- NP779580.RA_vIXlvgL_XexFiDE3cgEx8TpHogomg0akL-95Lr1Bnw130_assertion description "[The SOD2 Val/Val genotype may increase the risk of NSCLC carried by XRCC1 and p53 polymorphisms, particularly for adenocarcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP779580.RA_vIXlvgL_XexFiDE3cgEx8TpHogomg0akL-95Lr1Bnw130_provenance.
- NP779580.RA_vIXlvgL_XexFiDE3cgEx8TpHogomg0akL-95Lr1Bnw130_assertion evidence source_evidence_literature NP779580.RA_vIXlvgL_XexFiDE3cgEx8TpHogomg0akL-95Lr1Bnw130_provenance.
- NP779580.RA_vIXlvgL_XexFiDE3cgEx8TpHogomg0akL-95Lr1Bnw130_assertion SIO_000772 15534883 NP779580.RA_vIXlvgL_XexFiDE3cgEx8TpHogomg0akL-95Lr1Bnw130_provenance.
- NP779580.RA_vIXlvgL_XexFiDE3cgEx8TpHogomg0akL-95Lr1Bnw130_assertion wasDerivedFrom befree-20150227 NP779580.RA_vIXlvgL_XexFiDE3cgEx8TpHogomg0akL-95Lr1Bnw130_provenance.
- NP779580.RA_vIXlvgL_XexFiDE3cgEx8TpHogomg0akL-95Lr1Bnw130_assertion wasGeneratedBy ECO_0000203 NP779580.RA_vIXlvgL_XexFiDE3cgEx8TpHogomg0akL-95Lr1Bnw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP779580.RA_vIXlvgL_XexFiDE3cgEx8TpHogomg0akL-95Lr1Bnw130_provenance.