Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP56022.RANrzCOSiYM8pWrBxBAf9r_d0Ffqsy3HJKIuctr7k0LkQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP56022.RANrzCOSiYM8pWrBxBAf9r_d0Ffqsy3HJKIuctr7k0LkQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP56022.RANrzCOSiYM8pWrBxBAf9r_d0Ffqsy3HJKIuctr7k0LkQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP56022.RANrzCOSiYM8pWrBxBAf9r_d0Ffqsy3HJKIuctr7k0LkQ130_provenance.
- NP56022.RANrzCOSiYM8pWrBxBAf9r_d0Ffqsy3HJKIuctr7k0LkQ130_assertion description "[There were no statistically significant allele or haplotype frequency differences between cases and controls. Therefore, these results provide no evidence that these loci are associated with CD in this sample population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP56022.RANrzCOSiYM8pWrBxBAf9r_d0Ffqsy3HJKIuctr7k0LkQ130_provenance.
- NP56022.RANrzCOSiYM8pWrBxBAf9r_d0Ffqsy3HJKIuctr7k0LkQ130_assertion evidence source_evidence_literature NP56022.RANrzCOSiYM8pWrBxBAf9r_d0Ffqsy3HJKIuctr7k0LkQ130_provenance.
- NP56022.RANrzCOSiYM8pWrBxBAf9r_d0Ffqsy3HJKIuctr7k0LkQ130_assertion SIO_000772 15713213 NP56022.RANrzCOSiYM8pWrBxBAf9r_d0Ffqsy3HJKIuctr7k0LkQ130_provenance.
- NP56022.RANrzCOSiYM8pWrBxBAf9r_d0Ffqsy3HJKIuctr7k0LkQ130_assertion wasDerivedFrom gad-20130706 NP56022.RANrzCOSiYM8pWrBxBAf9r_d0Ffqsy3HJKIuctr7k0LkQ130_provenance.
- NP56022.RANrzCOSiYM8pWrBxBAf9r_d0Ffqsy3HJKIuctr7k0LkQ130_assertion wasGeneratedBy ECO_0000203 NP56022.RANrzCOSiYM8pWrBxBAf9r_d0Ffqsy3HJKIuctr7k0LkQ130_provenance.
- gad-20130706 importedOn "2013-07-06" NP56022.RANrzCOSiYM8pWrBxBAf9r_d0Ffqsy3HJKIuctr7k0LkQ130_provenance.