Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP309215.RAFZ0IXVcyQ5oR3sNGax11_mIlYJmRHT-a1ZSqInoO5Mk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP309215.RAFZ0IXVcyQ5oR3sNGax11_mIlYJmRHT-a1ZSqInoO5Mk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP309215.RAFZ0IXVcyQ5oR3sNGax11_mIlYJmRHT-a1ZSqInoO5Mk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP309215.RAFZ0IXVcyQ5oR3sNGax11_mIlYJmRHT-a1ZSqInoO5Mk130_provenance.
- NP309215.RAFZ0IXVcyQ5oR3sNGax11_mIlYJmRHT-a1ZSqInoO5Mk130_assertion description "[Both ecNOS a/b and p22 phox C242T polymorphisms were found to be associated with the development of CAD in the study population (p=0.020 and 0.011, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP309215.RAFZ0IXVcyQ5oR3sNGax11_mIlYJmRHT-a1ZSqInoO5Mk130_provenance.
- NP309215.RAFZ0IXVcyQ5oR3sNGax11_mIlYJmRHT-a1ZSqInoO5Mk130_assertion evidence source_evidence_literature NP309215.RAFZ0IXVcyQ5oR3sNGax11_mIlYJmRHT-a1ZSqInoO5Mk130_provenance.
- NP309215.RAFZ0IXVcyQ5oR3sNGax11_mIlYJmRHT-a1ZSqInoO5Mk130_assertion SIO_000772 11530961 NP309215.RAFZ0IXVcyQ5oR3sNGax11_mIlYJmRHT-a1ZSqInoO5Mk130_provenance.
- NP309215.RAFZ0IXVcyQ5oR3sNGax11_mIlYJmRHT-a1ZSqInoO5Mk130_assertion wasDerivedFrom befree-20140225 NP309215.RAFZ0IXVcyQ5oR3sNGax11_mIlYJmRHT-a1ZSqInoO5Mk130_provenance.
- NP309215.RAFZ0IXVcyQ5oR3sNGax11_mIlYJmRHT-a1ZSqInoO5Mk130_assertion wasGeneratedBy ECO_0000203 NP309215.RAFZ0IXVcyQ5oR3sNGax11_mIlYJmRHT-a1ZSqInoO5Mk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP309215.RAFZ0IXVcyQ5oR3sNGax11_mIlYJmRHT-a1ZSqInoO5Mk130_provenance.