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- source_evidence_literature type ECO_0000212 NP326137.RA4SDPP5dko19MutE_nAqsR7QGd1Nkn4xKlCG94IZgFpQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP326137.RA4SDPP5dko19MutE_nAqsR7QGd1Nkn4xKlCG94IZgFpQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP326137.RA4SDPP5dko19MutE_nAqsR7QGd1Nkn4xKlCG94IZgFpQ130_provenance.
- NP326137.RA4SDPP5dko19MutE_nAqsR7QGd1Nkn4xKlCG94IZgFpQ130_assertion description "[In this study, we tested whether null genotypes for the GSTM1 and GSTT1 genes altered the risks for MDS, AML and AA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP326137.RA4SDPP5dko19MutE_nAqsR7QGd1Nkn4xKlCG94IZgFpQ130_provenance.
- NP326137.RA4SDPP5dko19MutE_nAqsR7QGd1Nkn4xKlCG94IZgFpQ130_assertion evidence source_evidence_literature NP326137.RA4SDPP5dko19MutE_nAqsR7QGd1Nkn4xKlCG94IZgFpQ130_provenance.
- NP326137.RA4SDPP5dko19MutE_nAqsR7QGd1Nkn4xKlCG94IZgFpQ130_assertion SIO_000772 11488937 NP326137.RA4SDPP5dko19MutE_nAqsR7QGd1Nkn4xKlCG94IZgFpQ130_provenance.
- NP326137.RA4SDPP5dko19MutE_nAqsR7QGd1Nkn4xKlCG94IZgFpQ130_assertion wasDerivedFrom befree-2016 NP326137.RA4SDPP5dko19MutE_nAqsR7QGd1Nkn4xKlCG94IZgFpQ130_provenance.
- NP326137.RA4SDPP5dko19MutE_nAqsR7QGd1Nkn4xKlCG94IZgFpQ130_assertion wasGeneratedBy ECO_0000203 NP326137.RA4SDPP5dko19MutE_nAqsR7QGd1Nkn4xKlCG94IZgFpQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP326137.RA4SDPP5dko19MutE_nAqsR7QGd1Nkn4xKlCG94IZgFpQ130_provenance.