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- source_evidence_literature type ECO_0000212 NP478524.RAHWMmo-JoHXdAZDUQQpuFA8AbQeV5omKaW4M2gSL07VA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478524.RAHWMmo-JoHXdAZDUQQpuFA8AbQeV5omKaW4M2gSL07VA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478524.RAHWMmo-JoHXdAZDUQQpuFA8AbQeV5omKaW4M2gSL07VA130_provenance.
- NP478524.RAHWMmo-JoHXdAZDUQQpuFA8AbQeV5omKaW4M2gSL07VA130_assertion description "[The risk for colorectal cancer did not appear to differ significantly amongst individuals featuring the XRCC1 399Arg/Arg genotype (OR = 1.18; 95% CI, 0.96-1.45), the XRCC3 241Thr/Thr genotype (OR = 1.25; 95% CI, 0.88-1.79) or the XPD 751Gln allele (OR = 1.20; 95% CI, 0.90-1.61), although individuals featuring a greater number of risk genotypes (genotype with OR greater than 1) did experience a higher risk for colorectal cancer when compared to those who didn't feature any risk genotypes (Trend test P = 0.03).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478524.RAHWMmo-JoHXdAZDUQQpuFA8AbQeV5omKaW4M2gSL07VA130_provenance.
- NP478524.RAHWMmo-JoHXdAZDUQQpuFA8AbQeV5omKaW4M2gSL07VA130_assertion evidence source_evidence_literature NP478524.RAHWMmo-JoHXdAZDUQQpuFA8AbQeV5omKaW4M2gSL07VA130_provenance.
- NP478524.RAHWMmo-JoHXdAZDUQQpuFA8AbQeV5omKaW4M2gSL07VA130_assertion SIO_000772 15679883 NP478524.RAHWMmo-JoHXdAZDUQQpuFA8AbQeV5omKaW4M2gSL07VA130_provenance.
- NP478524.RAHWMmo-JoHXdAZDUQQpuFA8AbQeV5omKaW4M2gSL07VA130_assertion wasDerivedFrom befree-2016 NP478524.RAHWMmo-JoHXdAZDUQQpuFA8AbQeV5omKaW4M2gSL07VA130_provenance.
- NP478524.RAHWMmo-JoHXdAZDUQQpuFA8AbQeV5omKaW4M2gSL07VA130_assertion wasGeneratedBy ECO_0000203 NP478524.RAHWMmo-JoHXdAZDUQQpuFA8AbQeV5omKaW4M2gSL07VA130_provenance.
- befree-2016 importedOn "2016-02-19" NP478524.RAHWMmo-JoHXdAZDUQQpuFA8AbQeV5omKaW4M2gSL07VA130_provenance.