Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP118206.RAgTq_IEOkctPMBn5slr5Y3xio_4afQI3QkNk9Xrnr5oM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP118206.RAgTq_IEOkctPMBn5slr5Y3xio_4afQI3QkNk9Xrnr5oM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP118206.RAgTq_IEOkctPMBn5slr5Y3xio_4afQI3QkNk9Xrnr5oM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP118206.RAgTq_IEOkctPMBn5slr5Y3xio_4afQI3QkNk9Xrnr5oM130_provenance.
- NP118206.RAgTq_IEOkctPMBn5slr5Y3xio_4afQI3QkNk9Xrnr5oM130_assertion description "[Compared with the PEMT GG genotype, the variant CC genotype was associated with an increased risk of breast cancer (OR: 1.30; 95% CI: 1.01-1.67).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP118206.RAgTq_IEOkctPMBn5slr5Y3xio_4afQI3QkNk9Xrnr5oM130_provenance.
- NP118206.RAgTq_IEOkctPMBn5slr5Y3xio_4afQI3QkNk9Xrnr5oM130_assertion evidence source_evidence_literature NP118206.RAgTq_IEOkctPMBn5slr5Y3xio_4afQI3QkNk9Xrnr5oM130_provenance.
- NP118206.RAgTq_IEOkctPMBn5slr5Y3xio_4afQI3QkNk9Xrnr5oM130_assertion SIO_000772 18230680 NP118206.RAgTq_IEOkctPMBn5slr5Y3xio_4afQI3QkNk9Xrnr5oM130_provenance.
- NP118206.RAgTq_IEOkctPMBn5slr5Y3xio_4afQI3QkNk9Xrnr5oM130_assertion wasDerivedFrom gad-20150221 NP118206.RAgTq_IEOkctPMBn5slr5Y3xio_4afQI3QkNk9Xrnr5oM130_provenance.
- NP118206.RAgTq_IEOkctPMBn5slr5Y3xio_4afQI3QkNk9Xrnr5oM130_assertion wasGeneratedBy ECO_0000203 NP118206.RAgTq_IEOkctPMBn5slr5Y3xio_4afQI3QkNk9Xrnr5oM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP118206.RAgTq_IEOkctPMBn5slr5Y3xio_4afQI3QkNk9Xrnr5oM130_provenance.