Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP634887.RAJRaROuCDuD32dr8skU2Te6Ef18q1brYdDb0D3U4EgXU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP634887.RAJRaROuCDuD32dr8skU2Te6Ef18q1brYdDb0D3U4EgXU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP634887.RAJRaROuCDuD32dr8skU2Te6Ef18q1brYdDb0D3U4EgXU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP634887.RAJRaROuCDuD32dr8skU2Te6Ef18q1brYdDb0D3U4EgXU130_provenance.
- NP634887.RAJRaROuCDuD32dr8skU2Te6Ef18q1brYdDb0D3U4EgXU130_assertion description "[As to GSTP1 and PON1 192 polymorphisms, the mutant Val and R alleles, respectively, were associated with a decreased risk of developing BC, while polymorphisms in PON1 55 and GLO1 were associated with an increased risk of this neoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP634887.RAJRaROuCDuD32dr8skU2Te6Ef18q1brYdDb0D3U4EgXU130_provenance.
- NP634887.RAJRaROuCDuD32dr8skU2Te6Ef18q1brYdDb0D3U4EgXU130_assertion evidence source_evidence_literature NP634887.RAJRaROuCDuD32dr8skU2Te6Ef18q1brYdDb0D3U4EgXU130_provenance.
- NP634887.RAJRaROuCDuD32dr8skU2Te6Ef18q1brYdDb0D3U4EgXU130_assertion SIO_000772 19379515 NP634887.RAJRaROuCDuD32dr8skU2Te6Ef18q1brYdDb0D3U4EgXU130_provenance.
- NP634887.RAJRaROuCDuD32dr8skU2Te6Ef18q1brYdDb0D3U4EgXU130_assertion wasDerivedFrom befree-20150227 NP634887.RAJRaROuCDuD32dr8skU2Te6Ef18q1brYdDb0D3U4EgXU130_provenance.
- NP634887.RAJRaROuCDuD32dr8skU2Te6Ef18q1brYdDb0D3U4EgXU130_assertion wasGeneratedBy ECO_0000203 NP634887.RAJRaROuCDuD32dr8skU2Te6Ef18q1brYdDb0D3U4EgXU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP634887.RAJRaROuCDuD32dr8skU2Te6Ef18q1brYdDb0D3U4EgXU130_provenance.