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- source_evidence_literature type ECO_0000212 NP129884.RAyx-Mv5_V9aPoRO2lpgi008_xZYHm5E2SYAJqzFmsyrA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP129884.RAyx-Mv5_V9aPoRO2lpgi008_xZYHm5E2SYAJqzFmsyrA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP129884.RAyx-Mv5_V9aPoRO2lpgi008_xZYHm5E2SYAJqzFmsyrA130_provenance.
- NP129884.RAyx-Mv5_V9aPoRO2lpgi008_xZYHm5E2SYAJqzFmsyrA130_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." NP129884.RAyx-Mv5_V9aPoRO2lpgi008_xZYHm5E2SYAJqzFmsyrA130_provenance.
- NP129884.RAyx-Mv5_V9aPoRO2lpgi008_xZYHm5E2SYAJqzFmsyrA130_assertion evidence source_evidence_literature NP129884.RAyx-Mv5_V9aPoRO2lpgi008_xZYHm5E2SYAJqzFmsyrA130_provenance.
- NP129884.RAyx-Mv5_V9aPoRO2lpgi008_xZYHm5E2SYAJqzFmsyrA130_assertion SIO_000772 20737570 NP129884.RAyx-Mv5_V9aPoRO2lpgi008_xZYHm5E2SYAJqzFmsyrA130_provenance.
- NP129884.RAyx-Mv5_V9aPoRO2lpgi008_xZYHm5E2SYAJqzFmsyrA130_assertion wasDerivedFrom gad-20150221 NP129884.RAyx-Mv5_V9aPoRO2lpgi008_xZYHm5E2SYAJqzFmsyrA130_provenance.
- NP129884.RAyx-Mv5_V9aPoRO2lpgi008_xZYHm5E2SYAJqzFmsyrA130_assertion wasGeneratedBy ECO_0000203 NP129884.RAyx-Mv5_V9aPoRO2lpgi008_xZYHm5E2SYAJqzFmsyrA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP129884.RAyx-Mv5_V9aPoRO2lpgi008_xZYHm5E2SYAJqzFmsyrA130_provenance.