Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP308857.RAXH99cyuL6hGrmUgTsXIP0FceKoLsTROKvMOCIEQVgCQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP308857.RAXH99cyuL6hGrmUgTsXIP0FceKoLsTROKvMOCIEQVgCQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP308857.RAXH99cyuL6hGrmUgTsXIP0FceKoLsTROKvMOCIEQVgCQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP308857.RAXH99cyuL6hGrmUgTsXIP0FceKoLsTROKvMOCIEQVgCQ130_provenance.
- NP308857.RAXH99cyuL6hGrmUgTsXIP0FceKoLsTROKvMOCIEQVgCQ130_assertion description "[Our results indicate that the SRD5A2 V89L VV genotype interacts with VDR FokI TT/CT genotypes in NHW men and VDR CDX2 GG genotypes in HW men to increase the risk for prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP308857.RAXH99cyuL6hGrmUgTsXIP0FceKoLsTROKvMOCIEQVgCQ130_provenance.
- NP308857.RAXH99cyuL6hGrmUgTsXIP0FceKoLsTROKvMOCIEQVgCQ130_assertion evidence source_evidence_literature NP308857.RAXH99cyuL6hGrmUgTsXIP0FceKoLsTROKvMOCIEQVgCQ130_provenance.
- NP308857.RAXH99cyuL6hGrmUgTsXIP0FceKoLsTROKvMOCIEQVgCQ130_assertion SIO_000772 18483391 NP308857.RAXH99cyuL6hGrmUgTsXIP0FceKoLsTROKvMOCIEQVgCQ130_provenance.
- NP308857.RAXH99cyuL6hGrmUgTsXIP0FceKoLsTROKvMOCIEQVgCQ130_assertion wasDerivedFrom befree-20150227 NP308857.RAXH99cyuL6hGrmUgTsXIP0FceKoLsTROKvMOCIEQVgCQ130_provenance.
- NP308857.RAXH99cyuL6hGrmUgTsXIP0FceKoLsTROKvMOCIEQVgCQ130_assertion wasGeneratedBy ECO_0000203 NP308857.RAXH99cyuL6hGrmUgTsXIP0FceKoLsTROKvMOCIEQVgCQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP308857.RAXH99cyuL6hGrmUgTsXIP0FceKoLsTROKvMOCIEQVgCQ130_provenance.