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- source_evidence_literature type ECO_0000212 NP878382.RAGPIkgns5PghyGWMpNB0dyYEje05SRSS85ugVO54mfFg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP878382.RAGPIkgns5PghyGWMpNB0dyYEje05SRSS85ugVO54mfFg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP878382.RAGPIkgns5PghyGWMpNB0dyYEje05SRSS85ugVO54mfFg130_provenance.
- befree-2016 importedOn "2016-02-19" NP878382.RAGPIkgns5PghyGWMpNB0dyYEje05SRSS85ugVO54mfFg130_provenance.
- NP878382.RAGPIkgns5PghyGWMpNB0dyYEje05SRSS85ugVO54mfFg130_assertion wasGeneratedBy ECO_0000203 NP878382.RAGPIkgns5PghyGWMpNB0dyYEje05SRSS85ugVO54mfFg130_provenance.
- NP878382.RAGPIkgns5PghyGWMpNB0dyYEje05SRSS85ugVO54mfFg130_assertion wasDerivedFrom befree-2016 NP878382.RAGPIkgns5PghyGWMpNB0dyYEje05SRSS85ugVO54mfFg130_provenance.
- NP878382.RAGPIkgns5PghyGWMpNB0dyYEje05SRSS85ugVO54mfFg130_assertion SIO_000772 21389716 NP878382.RAGPIkgns5PghyGWMpNB0dyYEje05SRSS85ugVO54mfFg130_provenance.
- NP878382.RAGPIkgns5PghyGWMpNB0dyYEje05SRSS85ugVO54mfFg130_assertion evidence source_evidence_literature NP878382.RAGPIkgns5PghyGWMpNB0dyYEje05SRSS85ugVO54mfFg130_provenance.
- NP878382.RAGPIkgns5PghyGWMpNB0dyYEje05SRSS85ugVO54mfFg130_assertion description "[When GST polymorphism was analyzed in patients with AMI, GSTM1 null genotype frequencies were 0.24 and 0.21 among cases with coronary artery disease and controls, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP878382.RAGPIkgns5PghyGWMpNB0dyYEje05SRSS85ugVO54mfFg130_provenance.