Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP168161.RA-B635CeLyOEDD7CDB1CmMLVB90sO4ogQiGqs8LAkgrQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP168161.RA-B635CeLyOEDD7CDB1CmMLVB90sO4ogQiGqs8LAkgrQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP168161.RA-B635CeLyOEDD7CDB1CmMLVB90sO4ogQiGqs8LAkgrQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP168161.RA-B635CeLyOEDD7CDB1CmMLVB90sO4ogQiGqs8LAkgrQ130_provenance.
- NP168161.RA-B635CeLyOEDD7CDB1CmMLVB90sO4ogQiGqs8LAkgrQ130_assertion description "[Subjects with the XRCC1 Gln/Gln genotype were inversely associated with adenoma risk (odds ratio, 0.6; 95% confidence interval, 0.4-0.9; P = 0.01) when compared with subjects with Arg/Arg and Arg/Gln genotypes combined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP168161.RA-B635CeLyOEDD7CDB1CmMLVB90sO4ogQiGqs8LAkgrQ130_provenance.
- NP168161.RA-B635CeLyOEDD7CDB1CmMLVB90sO4ogQiGqs8LAkgrQ130_assertion evidence source_evidence_literature NP168161.RA-B635CeLyOEDD7CDB1CmMLVB90sO4ogQiGqs8LAkgrQ130_provenance.
- NP168161.RA-B635CeLyOEDD7CDB1CmMLVB90sO4ogQiGqs8LAkgrQ130_assertion SIO_000772 15767338 NP168161.RA-B635CeLyOEDD7CDB1CmMLVB90sO4ogQiGqs8LAkgrQ130_provenance.
- NP168161.RA-B635CeLyOEDD7CDB1CmMLVB90sO4ogQiGqs8LAkgrQ130_assertion wasDerivedFrom befree-20140225 NP168161.RA-B635CeLyOEDD7CDB1CmMLVB90sO4ogQiGqs8LAkgrQ130_provenance.
- NP168161.RA-B635CeLyOEDD7CDB1CmMLVB90sO4ogQiGqs8LAkgrQ130_assertion wasGeneratedBy ECO_0000203 NP168161.RA-B635CeLyOEDD7CDB1CmMLVB90sO4ogQiGqs8LAkgrQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP168161.RA-B635CeLyOEDD7CDB1CmMLVB90sO4ogQiGqs8LAkgrQ130_provenance.