Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP887022.RAu1DAsNG4ro_kF1udhGRYSWboWQqXHAoSEM7NHlB3k14130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP887022.RAu1DAsNG4ro_kF1udhGRYSWboWQqXHAoSEM7NHlB3k14130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP887022.RAu1DAsNG4ro_kF1udhGRYSWboWQqXHAoSEM7NHlB3k14130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP887022.RAu1DAsNG4ro_kF1udhGRYSWboWQqXHAoSEM7NHlB3k14130_provenance.
- NP887022.RAu1DAsNG4ro_kF1udhGRYSWboWQqXHAoSEM7NHlB3k14130_assertion description "[Homozygote carriers of variant alleles for the PTGS1 50C>T, PTGS2 -765G>C and IL-10 -592C>A polymorphisms did not have a significantly altered risk of CRA recurrence (relative risk [RR]=0.91; 95% confidence interval [CI]: 0.14-6.07, RR=1.32; 95% CI: 0.66-2.62 and RR=1.24; 95% CI: 0.74-2.07, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887022.RAu1DAsNG4ro_kF1udhGRYSWboWQqXHAoSEM7NHlB3k14130_provenance.
- NP887022.RAu1DAsNG4ro_kF1udhGRYSWboWQqXHAoSEM7NHlB3k14130_assertion evidence source_evidence_literature NP887022.RAu1DAsNG4ro_kF1udhGRYSWboWQqXHAoSEM7NHlB3k14130_provenance.
- NP887022.RAu1DAsNG4ro_kF1udhGRYSWboWQqXHAoSEM7NHlB3k14130_assertion SIO_000772 17640058 NP887022.RAu1DAsNG4ro_kF1udhGRYSWboWQqXHAoSEM7NHlB3k14130_provenance.
- NP887022.RAu1DAsNG4ro_kF1udhGRYSWboWQqXHAoSEM7NHlB3k14130_assertion wasDerivedFrom befree-20140225 NP887022.RAu1DAsNG4ro_kF1udhGRYSWboWQqXHAoSEM7NHlB3k14130_provenance.
- NP887022.RAu1DAsNG4ro_kF1udhGRYSWboWQqXHAoSEM7NHlB3k14130_assertion wasGeneratedBy ECO_0000203 NP887022.RAu1DAsNG4ro_kF1udhGRYSWboWQqXHAoSEM7NHlB3k14130_provenance.
- befree-20140225 importedOn "2014-02-25" NP887022.RAu1DAsNG4ro_kF1udhGRYSWboWQqXHAoSEM7NHlB3k14130_provenance.