Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP691276.RAUaP82ULlUvb7bf3ac2mmAx73SA1mvUBDr9KOj854BZ4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP691276.RAUaP82ULlUvb7bf3ac2mmAx73SA1mvUBDr9KOj854BZ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP691276.RAUaP82ULlUvb7bf3ac2mmAx73SA1mvUBDr9KOj854BZ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP691276.RAUaP82ULlUvb7bf3ac2mmAx73SA1mvUBDr9KOj854BZ4130_provenance.
- NP691276.RAUaP82ULlUvb7bf3ac2mmAx73SA1mvUBDr9KOj854BZ4130_assertion description "[Both the Lig4 c.26 and the Rad51 c.-3429 polymorphisms were associated with a significant reduced risk for HNSCC (OR=0.43, p=0.01; OR=0.43, p=0.05 respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP691276.RAUaP82ULlUvb7bf3ac2mmAx73SA1mvUBDr9KOj854BZ4130_provenance.
- NP691276.RAUaP82ULlUvb7bf3ac2mmAx73SA1mvUBDr9KOj854BZ4130_assertion evidence source_evidence_literature NP691276.RAUaP82ULlUvb7bf3ac2mmAx73SA1mvUBDr9KOj854BZ4130_provenance.
- NP691276.RAUaP82ULlUvb7bf3ac2mmAx73SA1mvUBDr9KOj854BZ4130_assertion SIO_000772 18768166 NP691276.RAUaP82ULlUvb7bf3ac2mmAx73SA1mvUBDr9KOj854BZ4130_provenance.
- NP691276.RAUaP82ULlUvb7bf3ac2mmAx73SA1mvUBDr9KOj854BZ4130_assertion wasDerivedFrom befree-2016 NP691276.RAUaP82ULlUvb7bf3ac2mmAx73SA1mvUBDr9KOj854BZ4130_provenance.
- NP691276.RAUaP82ULlUvb7bf3ac2mmAx73SA1mvUBDr9KOj854BZ4130_assertion wasGeneratedBy ECO_0000203 NP691276.RAUaP82ULlUvb7bf3ac2mmAx73SA1mvUBDr9KOj854BZ4130_provenance.
- befree-2016 importedOn "2016-02-19" NP691276.RAUaP82ULlUvb7bf3ac2mmAx73SA1mvUBDr9KOj854BZ4130_provenance.