Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP190340.RAvNNhCoTGgZUsqiFr5Ftvo-UXiqv2DOIwzScpLCVJiyg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP190340.RAvNNhCoTGgZUsqiFr5Ftvo-UXiqv2DOIwzScpLCVJiyg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP190340.RAvNNhCoTGgZUsqiFr5Ftvo-UXiqv2DOIwzScpLCVJiyg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP190340.RAvNNhCoTGgZUsqiFr5Ftvo-UXiqv2DOIwzScpLCVJiyg130_provenance.
- NP190340.RAvNNhCoTGgZUsqiFr5Ftvo-UXiqv2DOIwzScpLCVJiyg130_assertion description "[To further define the genetic basis of narcolepsy risk, we performed a genome-wide association study (GWAS) in 562 European individuals with narcolepsy (cases) and 702 ethnically matched controls, with independent replication in 370 cases and 495 controls, all heterozygous for DRB1*1501-DQB1*0602.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP190340.RAvNNhCoTGgZUsqiFr5Ftvo-UXiqv2DOIwzScpLCVJiyg130_provenance.
- NP190340.RAvNNhCoTGgZUsqiFr5Ftvo-UXiqv2DOIwzScpLCVJiyg130_assertion evidence source_evidence_literature NP190340.RAvNNhCoTGgZUsqiFr5Ftvo-UXiqv2DOIwzScpLCVJiyg130_provenance.
- NP190340.RAvNNhCoTGgZUsqiFr5Ftvo-UXiqv2DOIwzScpLCVJiyg130_assertion SIO_000772 20711174 NP190340.RAvNNhCoTGgZUsqiFr5Ftvo-UXiqv2DOIwzScpLCVJiyg130_provenance.
- NP190340.RAvNNhCoTGgZUsqiFr5Ftvo-UXiqv2DOIwzScpLCVJiyg130_assertion wasDerivedFrom befree-20140225 NP190340.RAvNNhCoTGgZUsqiFr5Ftvo-UXiqv2DOIwzScpLCVJiyg130_provenance.
- NP190340.RAvNNhCoTGgZUsqiFr5Ftvo-UXiqv2DOIwzScpLCVJiyg130_assertion wasGeneratedBy ECO_0000203 NP190340.RAvNNhCoTGgZUsqiFr5Ftvo-UXiqv2DOIwzScpLCVJiyg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP190340.RAvNNhCoTGgZUsqiFr5Ftvo-UXiqv2DOIwzScpLCVJiyg130_provenance.