Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP209216.RAD4U5GOz05iWNIoFtTcQueo4EWeRNmDHHpWHSxk7pWVw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP209216.RAD4U5GOz05iWNIoFtTcQueo4EWeRNmDHHpWHSxk7pWVw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP209216.RAD4U5GOz05iWNIoFtTcQueo4EWeRNmDHHpWHSxk7pWVw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP209216.RAD4U5GOz05iWNIoFtTcQueo4EWeRNmDHHpWHSxk7pWVw130_provenance.
- NP209216.RAD4U5GOz05iWNIoFtTcQueo4EWeRNmDHHpWHSxk7pWVw130_assertion description "[Carriers of the variant allele of MDR1 intron 3 polymorphism were at 1.52-fold higher risk of CRC than homozygous wild type allele carriers (Incidence rate ratio (IRR) = 1.52, 95% Confidence Interval (CI): 1.12-2.06).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209216.RAD4U5GOz05iWNIoFtTcQueo4EWeRNmDHHpWHSxk7pWVw130_provenance.
- NP209216.RAD4U5GOz05iWNIoFtTcQueo4EWeRNmDHHpWHSxk7pWVw130_assertion evidence source_evidence_literature NP209216.RAD4U5GOz05iWNIoFtTcQueo4EWeRNmDHHpWHSxk7pWVw130_provenance.
- NP209216.RAD4U5GOz05iWNIoFtTcQueo4EWeRNmDHHpWHSxk7pWVw130_assertion SIO_000772 19930591 NP209216.RAD4U5GOz05iWNIoFtTcQueo4EWeRNmDHHpWHSxk7pWVw130_provenance.
- NP209216.RAD4U5GOz05iWNIoFtTcQueo4EWeRNmDHHpWHSxk7pWVw130_assertion wasDerivedFrom befree-20140225 NP209216.RAD4U5GOz05iWNIoFtTcQueo4EWeRNmDHHpWHSxk7pWVw130_provenance.
- NP209216.RAD4U5GOz05iWNIoFtTcQueo4EWeRNmDHHpWHSxk7pWVw130_assertion wasGeneratedBy ECO_0000203 NP209216.RAD4U5GOz05iWNIoFtTcQueo4EWeRNmDHHpWHSxk7pWVw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP209216.RAD4U5GOz05iWNIoFtTcQueo4EWeRNmDHHpWHSxk7pWVw130_provenance.