Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP471163.RAgvBTLGrxSXjavzGz8aX6VwKBPsSSJh-NYP9rUFWplss130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP471163.RAgvBTLGrxSXjavzGz8aX6VwKBPsSSJh-NYP9rUFWplss130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP471163.RAgvBTLGrxSXjavzGz8aX6VwKBPsSSJh-NYP9rUFWplss130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP471163.RAgvBTLGrxSXjavzGz8aX6VwKBPsSSJh-NYP9rUFWplss130_provenance.
- NP471163.RAgvBTLGrxSXjavzGz8aX6VwKBPsSSJh-NYP9rUFWplss130_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." NP471163.RAgvBTLGrxSXjavzGz8aX6VwKBPsSSJh-NYP9rUFWplss130_provenance.
- NP471163.RAgvBTLGrxSXjavzGz8aX6VwKBPsSSJh-NYP9rUFWplss130_assertion evidence source_evidence_literature NP471163.RAgvBTLGrxSXjavzGz8aX6VwKBPsSSJh-NYP9rUFWplss130_provenance.
- NP471163.RAgvBTLGrxSXjavzGz8aX6VwKBPsSSJh-NYP9rUFWplss130_assertion SIO_000772 18230680 NP471163.RAgvBTLGrxSXjavzGz8aX6VwKBPsSSJh-NYP9rUFWplss130_provenance.
- NP471163.RAgvBTLGrxSXjavzGz8aX6VwKBPsSSJh-NYP9rUFWplss130_assertion wasDerivedFrom befree-20140225 NP471163.RAgvBTLGrxSXjavzGz8aX6VwKBPsSSJh-NYP9rUFWplss130_provenance.
- NP471163.RAgvBTLGrxSXjavzGz8aX6VwKBPsSSJh-NYP9rUFWplss130_assertion wasGeneratedBy ECO_0000203 NP471163.RAgvBTLGrxSXjavzGz8aX6VwKBPsSSJh-NYP9rUFWplss130_provenance.
- befree-20140225 importedOn "2014-02-25" NP471163.RAgvBTLGrxSXjavzGz8aX6VwKBPsSSJh-NYP9rUFWplss130_provenance.