Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP889930.RAmF8hrNvLfT40ubP_OFi0zAcu12poWAXqJO85GHy_MvY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP889930.RAmF8hrNvLfT40ubP_OFi0zAcu12poWAXqJO85GHy_MvY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP889930.RAmF8hrNvLfT40ubP_OFi0zAcu12poWAXqJO85GHy_MvY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP889930.RAmF8hrNvLfT40ubP_OFi0zAcu12poWAXqJO85GHy_MvY130_provenance.
- NP889930.RAmF8hrNvLfT40ubP_OFi0zAcu12poWAXqJO85GHy_MvY130_assertion description "[Carriers of the variant allele of MDR1 C3435T exon 26 had a lower risk of CRC than homozygous C-allele carriers (IRR = 0.71 (CI:0.50-1.00)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889930.RAmF8hrNvLfT40ubP_OFi0zAcu12poWAXqJO85GHy_MvY130_provenance.
- NP889930.RAmF8hrNvLfT40ubP_OFi0zAcu12poWAXqJO85GHy_MvY130_assertion evidence source_evidence_literature NP889930.RAmF8hrNvLfT40ubP_OFi0zAcu12poWAXqJO85GHy_MvY130_provenance.
- NP889930.RAmF8hrNvLfT40ubP_OFi0zAcu12poWAXqJO85GHy_MvY130_assertion SIO_000772 19930591 NP889930.RAmF8hrNvLfT40ubP_OFi0zAcu12poWAXqJO85GHy_MvY130_provenance.
- NP889930.RAmF8hrNvLfT40ubP_OFi0zAcu12poWAXqJO85GHy_MvY130_assertion wasDerivedFrom befree-20140225 NP889930.RAmF8hrNvLfT40ubP_OFi0zAcu12poWAXqJO85GHy_MvY130_provenance.
- NP889930.RAmF8hrNvLfT40ubP_OFi0zAcu12poWAXqJO85GHy_MvY130_assertion wasGeneratedBy ECO_0000203 NP889930.RAmF8hrNvLfT40ubP_OFi0zAcu12poWAXqJO85GHy_MvY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP889930.RAmF8hrNvLfT40ubP_OFi0zAcu12poWAXqJO85GHy_MvY130_provenance.