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- source_evidence_literature type ECO_0000212 NP493398.RAK1V4yHp4_OV-tQyunHDpJ5r8P1ijyZ8Uc8KC3Wm5548130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP493398.RAK1V4yHp4_OV-tQyunHDpJ5r8P1ijyZ8Uc8KC3Wm5548130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP493398.RAK1V4yHp4_OV-tQyunHDpJ5r8P1ijyZ8Uc8KC3Wm5548130_provenance.
- NP493398.RAK1V4yHp4_OV-tQyunHDpJ5r8P1ijyZ8Uc8KC3Wm5548130_assertion description "[GSTM1 null (GSTM1(-)) genotype frequencies in CML cases and controls were 45.3% and 42.6%, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP493398.RAK1V4yHp4_OV-tQyunHDpJ5r8P1ijyZ8Uc8KC3Wm5548130_provenance.
- NP493398.RAK1V4yHp4_OV-tQyunHDpJ5r8P1ijyZ8Uc8KC3Wm5548130_assertion evidence source_evidence_literature NP493398.RAK1V4yHp4_OV-tQyunHDpJ5r8P1ijyZ8Uc8KC3Wm5548130_provenance.
- NP493398.RAK1V4yHp4_OV-tQyunHDpJ5r8P1ijyZ8Uc8KC3Wm5548130_assertion SIO_000772 21969307 NP493398.RAK1V4yHp4_OV-tQyunHDpJ5r8P1ijyZ8Uc8KC3Wm5548130_provenance.
- NP493398.RAK1V4yHp4_OV-tQyunHDpJ5r8P1ijyZ8Uc8KC3Wm5548130_assertion wasDerivedFrom befree-20140225 NP493398.RAK1V4yHp4_OV-tQyunHDpJ5r8P1ijyZ8Uc8KC3Wm5548130_provenance.
- NP493398.RAK1V4yHp4_OV-tQyunHDpJ5r8P1ijyZ8Uc8KC3Wm5548130_assertion wasGeneratedBy ECO_0000203 NP493398.RAK1V4yHp4_OV-tQyunHDpJ5r8P1ijyZ8Uc8KC3Wm5548130_provenance.
- befree-20140225 importedOn "2014-02-25" NP493398.RAK1V4yHp4_OV-tQyunHDpJ5r8P1ijyZ8Uc8KC3Wm5548130_provenance.