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- source_evidence_literature type ECO_0000212 NP115039.RAro5UXEhwC55sc9rnnQGkXOsb_Crr7KAoOnqxlFvxDWw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP115039.RAro5UXEhwC55sc9rnnQGkXOsb_Crr7KAoOnqxlFvxDWw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP115039.RAro5UXEhwC55sc9rnnQGkXOsb_Crr7KAoOnqxlFvxDWw130_provenance.
- NP115039.RAro5UXEhwC55sc9rnnQGkXOsb_Crr7KAoOnqxlFvxDWw130_assertion description "[The analysis of binary genotype combinations showed increased colorectal cancer risk in individuals simultaneously homozygous for the variant alleles of APE1 Asn148Glu and hOGG1 Ser326Cys (OR: 6.37; 95% CI: 1.40-29.02; p=0.02).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP115039.RAro5UXEhwC55sc9rnnQGkXOsb_Crr7KAoOnqxlFvxDWw130_provenance.
- NP115039.RAro5UXEhwC55sc9rnnQGkXOsb_Crr7KAoOnqxlFvxDWw130_assertion evidence source_evidence_literature NP115039.RAro5UXEhwC55sc9rnnQGkXOsb_Crr7KAoOnqxlFvxDWw130_provenance.
- NP115039.RAro5UXEhwC55sc9rnnQGkXOsb_Crr7KAoOnqxlFvxDWw130_assertion SIO_000772 17991492 NP115039.RAro5UXEhwC55sc9rnnQGkXOsb_Crr7KAoOnqxlFvxDWw130_provenance.
- NP115039.RAro5UXEhwC55sc9rnnQGkXOsb_Crr7KAoOnqxlFvxDWw130_assertion wasDerivedFrom gad-20150221 NP115039.RAro5UXEhwC55sc9rnnQGkXOsb_Crr7KAoOnqxlFvxDWw130_provenance.
- NP115039.RAro5UXEhwC55sc9rnnQGkXOsb_Crr7KAoOnqxlFvxDWw130_assertion wasGeneratedBy ECO_0000203 NP115039.RAro5UXEhwC55sc9rnnQGkXOsb_Crr7KAoOnqxlFvxDWw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP115039.RAro5UXEhwC55sc9rnnQGkXOsb_Crr7KAoOnqxlFvxDWw130_provenance.