Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP642424.RAxmXNoKqB5X6YMJc5W3Oawu1Oynmd6GW6F4uL7pQGRoQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP642424.RAxmXNoKqB5X6YMJc5W3Oawu1Oynmd6GW6F4uL7pQGRoQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP642424.RAxmXNoKqB5X6YMJc5W3Oawu1Oynmd6GW6F4uL7pQGRoQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP642424.RAxmXNoKqB5X6YMJc5W3Oawu1Oynmd6GW6F4uL7pQGRoQ130_provenance.
- NP642424.RAxmXNoKqB5X6YMJc5W3Oawu1Oynmd6GW6F4uL7pQGRoQ130_assertion description "[However, as regard PON1 Q192R, the R mutated allele frequency was found in 28.5% in BC patients and in 33% in controls, the women who were QR heterozygotes (OR(adj) 0.96, 95% CI 0.55-1.68) or RR homozygotes (OR(adj) 0.64, 95% CI 0.25-1.63), and R allele (OR(adj) 0.81, 95% CI 0.53-1.42) did not show any risk for BC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP642424.RAxmXNoKqB5X6YMJc5W3Oawu1Oynmd6GW6F4uL7pQGRoQ130_provenance.
- NP642424.RAxmXNoKqB5X6YMJc5W3Oawu1Oynmd6GW6F4uL7pQGRoQ130_assertion evidence source_evidence_literature NP642424.RAxmXNoKqB5X6YMJc5W3Oawu1Oynmd6GW6F4uL7pQGRoQ130_provenance.
- NP642424.RAxmXNoKqB5X6YMJc5W3Oawu1Oynmd6GW6F4uL7pQGRoQ130_assertion SIO_000772 21229382 NP642424.RAxmXNoKqB5X6YMJc5W3Oawu1Oynmd6GW6F4uL7pQGRoQ130_provenance.
- NP642424.RAxmXNoKqB5X6YMJc5W3Oawu1Oynmd6GW6F4uL7pQGRoQ130_assertion wasDerivedFrom befree-20140225 NP642424.RAxmXNoKqB5X6YMJc5W3Oawu1Oynmd6GW6F4uL7pQGRoQ130_provenance.
- NP642424.RAxmXNoKqB5X6YMJc5W3Oawu1Oynmd6GW6F4uL7pQGRoQ130_assertion wasGeneratedBy ECO_0000203 NP642424.RAxmXNoKqB5X6YMJc5W3Oawu1Oynmd6GW6F4uL7pQGRoQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP642424.RAxmXNoKqB5X6YMJc5W3Oawu1Oynmd6GW6F4uL7pQGRoQ130_provenance.