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- source_evidence_literature type ECO_0000212 NP832699.RAoziLkkfk-IM3c33UQQ5H5E-Mg3vduWypoB0TnAbfgH8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP832699.RAoziLkkfk-IM3c33UQQ5H5E-Mg3vduWypoB0TnAbfgH8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP832699.RAoziLkkfk-IM3c33UQQ5H5E-Mg3vduWypoB0TnAbfgH8130_provenance.
- NP832699.RAoziLkkfk-IM3c33UQQ5H5E-Mg3vduWypoB0TnAbfgH8130_assertion description "[An SNP, Val83Met, in the MTH1 (microtT homolog 1) gene encoding a triphosphatase that hydrolyzes pro-mutagenic oxidized nucleoside triphosphates, such as 8-hydroxy-dGTP and 2-hydroxy-dATP, showed the strongest and a significant association with SCLC risk [odds ratio (OR)=1.6, 95% confidence interval (CI): 1.2-2.2, P=0.004], while three other SNPs in the TP53, BLM and SNM1 genes, respectively, also showed marginal associations (0.05<P<0.1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP832699.RAoziLkkfk-IM3c33UQQ5H5E-Mg3vduWypoB0TnAbfgH8130_provenance.
- NP832699.RAoziLkkfk-IM3c33UQQ5H5E-Mg3vduWypoB0TnAbfgH8130_assertion evidence source_evidence_literature NP832699.RAoziLkkfk-IM3c33UQQ5H5E-Mg3vduWypoB0TnAbfgH8130_provenance.
- NP832699.RAoziLkkfk-IM3c33UQQ5H5E-Mg3vduWypoB0TnAbfgH8130_assertion SIO_000772 16774934 NP832699.RAoziLkkfk-IM3c33UQQ5H5E-Mg3vduWypoB0TnAbfgH8130_provenance.
- NP832699.RAoziLkkfk-IM3c33UQQ5H5E-Mg3vduWypoB0TnAbfgH8130_assertion wasDerivedFrom befree-20150227 NP832699.RAoziLkkfk-IM3c33UQQ5H5E-Mg3vduWypoB0TnAbfgH8130_provenance.
- NP832699.RAoziLkkfk-IM3c33UQQ5H5E-Mg3vduWypoB0TnAbfgH8130_assertion wasGeneratedBy ECO_0000203 NP832699.RAoziLkkfk-IM3c33UQQ5H5E-Mg3vduWypoB0TnAbfgH8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP832699.RAoziLkkfk-IM3c33UQQ5H5E-Mg3vduWypoB0TnAbfgH8130_provenance.