Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP130042.RAs9mCz9Wl6mForQFi0Q7NEBvPBZRVuKKiY38Jcdj_oAM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP130042.RAs9mCz9Wl6mForQFi0Q7NEBvPBZRVuKKiY38Jcdj_oAM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP130042.RAs9mCz9Wl6mForQFi0Q7NEBvPBZRVuKKiY38Jcdj_oAM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP130042.RAs9mCz9Wl6mForQFi0Q7NEBvPBZRVuKKiY38Jcdj_oAM130_provenance.
- NP130042.RAs9mCz9Wl6mForQFi0Q7NEBvPBZRVuKKiY38Jcdj_oAM130_assertion description "[Variant alleles were significantly associated with favorable survivals of NSCLC for MTR rs3768160 A>G (allelic hazards ratio HR, 0.78; 95% confidence interval CI, 0.62-0.98), MTRR rs2966952 G>A (allelic HR, 0.84; 95% CI, 0.71-0.99) and DHFR rs1650697 G>A (allelic HR, 0.83; 95% CI, 0.70-0.99) and with unfavorable prognosis for MTHFD1 rs1950902 G>A with borderline significance (allelic HR, 1.18; 95% CI, 0.99-1.40).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130042.RAs9mCz9Wl6mForQFi0Q7NEBvPBZRVuKKiY38Jcdj_oAM130_provenance.
- NP130042.RAs9mCz9Wl6mForQFi0Q7NEBvPBZRVuKKiY38Jcdj_oAM130_assertion evidence source_evidence_literature NP130042.RAs9mCz9Wl6mForQFi0Q7NEBvPBZRVuKKiY38Jcdj_oAM130_provenance.
- NP130042.RAs9mCz9Wl6mForQFi0Q7NEBvPBZRVuKKiY38Jcdj_oAM130_assertion SIO_000772 20737570 NP130042.RAs9mCz9Wl6mForQFi0Q7NEBvPBZRVuKKiY38Jcdj_oAM130_provenance.
- NP130042.RAs9mCz9Wl6mForQFi0Q7NEBvPBZRVuKKiY38Jcdj_oAM130_assertion wasDerivedFrom gad-20150221 NP130042.RAs9mCz9Wl6mForQFi0Q7NEBvPBZRVuKKiY38Jcdj_oAM130_provenance.
- NP130042.RAs9mCz9Wl6mForQFi0Q7NEBvPBZRVuKKiY38Jcdj_oAM130_assertion wasGeneratedBy ECO_0000203 NP130042.RAs9mCz9Wl6mForQFi0Q7NEBvPBZRVuKKiY38Jcdj_oAM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP130042.RAs9mCz9Wl6mForQFi0Q7NEBvPBZRVuKKiY38Jcdj_oAM130_provenance.