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- source_evidence_literature type ECO_0000212 NP339156.RAn_ER0mBiVdxFZGNZi9xNryo1Y61WauIafjQP3jng0Sg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP339156.RAn_ER0mBiVdxFZGNZi9xNryo1Y61WauIafjQP3jng0Sg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP339156.RAn_ER0mBiVdxFZGNZi9xNryo1Y61WauIafjQP3jng0Sg130_provenance.
- NP339156.RAn_ER0mBiVdxFZGNZi9xNryo1Y61WauIafjQP3jng0Sg130_assertion description "[The impact of combined genotypes of the CYP1A1 Ile/Val polymorphism and GSTM1 on mutation of K-ras was also analyzed, and a higher risk of having a mutated K-ras gene was found for both the CYP1A1 Ile/Ile and GSTM1(-) (OR, 6.32; p=0.021; 95% CI, 1.33-30.19) and CYP1A1 Ile/Val and GSTM1(-) (OR, 6.09; p=0.042; 95% CI, 1.07-34.72) genotype combinations in patients with adenocarcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP339156.RAn_ER0mBiVdxFZGNZi9xNryo1Y61WauIafjQP3jng0Sg130_provenance.
- NP339156.RAn_ER0mBiVdxFZGNZi9xNryo1Y61WauIafjQP3jng0Sg130_assertion evidence source_evidence_literature NP339156.RAn_ER0mBiVdxFZGNZi9xNryo1Y61WauIafjQP3jng0Sg130_provenance.
- NP339156.RAn_ER0mBiVdxFZGNZi9xNryo1Y61WauIafjQP3jng0Sg130_assertion SIO_000772 15375499 NP339156.RAn_ER0mBiVdxFZGNZi9xNryo1Y61WauIafjQP3jng0Sg130_provenance.
- NP339156.RAn_ER0mBiVdxFZGNZi9xNryo1Y61WauIafjQP3jng0Sg130_assertion wasDerivedFrom befree-20150227 NP339156.RAn_ER0mBiVdxFZGNZi9xNryo1Y61WauIafjQP3jng0Sg130_provenance.
- NP339156.RAn_ER0mBiVdxFZGNZi9xNryo1Y61WauIafjQP3jng0Sg130_assertion wasGeneratedBy ECO_0000203 NP339156.RAn_ER0mBiVdxFZGNZi9xNryo1Y61WauIafjQP3jng0Sg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP339156.RAn_ER0mBiVdxFZGNZi9xNryo1Y61WauIafjQP3jng0Sg130_provenance.