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- source_evidence_literature type ECO_0000212 NP593092.RAnM81KNqaJM_libaBFEpLOoR0IATDuwuFPQkqOyqL76U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP593092.RAnM81KNqaJM_libaBFEpLOoR0IATDuwuFPQkqOyqL76U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP593092.RAnM81KNqaJM_libaBFEpLOoR0IATDuwuFPQkqOyqL76U130_provenance.
- befree-2016 importedOn "2016-02-19" NP593092.RAnM81KNqaJM_libaBFEpLOoR0IATDuwuFPQkqOyqL76U130_provenance.
- NP593092.RAnM81KNqaJM_libaBFEpLOoR0IATDuwuFPQkqOyqL76U130_assertion wasGeneratedBy ECO_0000203 NP593092.RAnM81KNqaJM_libaBFEpLOoR0IATDuwuFPQkqOyqL76U130_provenance.
- NP593092.RAnM81KNqaJM_libaBFEpLOoR0IATDuwuFPQkqOyqL76U130_assertion wasDerivedFrom befree-2016 NP593092.RAnM81KNqaJM_libaBFEpLOoR0IATDuwuFPQkqOyqL76U130_provenance.
- NP593092.RAnM81KNqaJM_libaBFEpLOoR0IATDuwuFPQkqOyqL76U130_assertion SIO_000772 17290392 NP593092.RAnM81KNqaJM_libaBFEpLOoR0IATDuwuFPQkqOyqL76U130_provenance.
- NP593092.RAnM81KNqaJM_libaBFEpLOoR0IATDuwuFPQkqOyqL76U130_assertion evidence source_evidence_literature NP593092.RAnM81KNqaJM_libaBFEpLOoR0IATDuwuFPQkqOyqL76U130_provenance.
- NP593092.RAnM81KNqaJM_libaBFEpLOoR0IATDuwuFPQkqOyqL76U130_assertion description "[An increased risk of MPM was found in subjects bearing a GSTM1 null allele (OR = 1.69, 95% CI = 1.04-2.74; p = 0.034), and in those with the Ala/Ala genotypes at codon 16 within MnSOD (OR = 3.07, 95% CI = 1.55-6.05; p = 0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP593092.RAnM81KNqaJM_libaBFEpLOoR0IATDuwuFPQkqOyqL76U130_provenance.