Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP78259.RAvOtq5_VeSFeR2IhCYP16uhVfrzSVy0GjKOCD2VELoJk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP78259.RAvOtq5_VeSFeR2IhCYP16uhVfrzSVy0GjKOCD2VELoJk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP78259.RAvOtq5_VeSFeR2IhCYP16uhVfrzSVy0GjKOCD2VELoJk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP78259.RAvOtq5_VeSFeR2IhCYP16uhVfrzSVy0GjKOCD2VELoJk130_provenance.
- NP78259.RAvOtq5_VeSFeR2IhCYP16uhVfrzSVy0GjKOCD2VELoJk130_assertion description "[Several other SNPs in the candidate genes, such as CTLA4, HAVCR1, and SUMO4, also had rather small p-values (<0.05), suggesting the associations between them and RA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78259.RAvOtq5_VeSFeR2IhCYP16uhVfrzSVy0GjKOCD2VELoJk130_provenance.
- NP78259.RAvOtq5_VeSFeR2IhCYP16uhVfrzSVy0GjKOCD2VELoJk130_assertion evidence source_evidence_literature NP78259.RAvOtq5_VeSFeR2IhCYP16uhVfrzSVy0GjKOCD2VELoJk130_provenance.
- NP78259.RAvOtq5_VeSFeR2IhCYP16uhVfrzSVy0GjKOCD2VELoJk130_assertion SIO_000772 18466531 NP78259.RAvOtq5_VeSFeR2IhCYP16uhVfrzSVy0GjKOCD2VELoJk130_provenance.
- NP78259.RAvOtq5_VeSFeR2IhCYP16uhVfrzSVy0GjKOCD2VELoJk130_assertion wasDerivedFrom gad-20130706 NP78259.RAvOtq5_VeSFeR2IhCYP16uhVfrzSVy0GjKOCD2VELoJk130_provenance.
- NP78259.RAvOtq5_VeSFeR2IhCYP16uhVfrzSVy0GjKOCD2VELoJk130_assertion wasGeneratedBy ECO_0000203 NP78259.RAvOtq5_VeSFeR2IhCYP16uhVfrzSVy0GjKOCD2VELoJk130_provenance.
- gad-20130706 importedOn "2013-07-06" NP78259.RAvOtq5_VeSFeR2IhCYP16uhVfrzSVy0GjKOCD2VELoJk130_provenance.