Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP17166.RAnq1Qv7cvzzHztdsZdAWshXEwvkdclZMXblD2PF7RC-g130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP17166.RAnq1Qv7cvzzHztdsZdAWshXEwvkdclZMXblD2PF7RC-g130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP17166.RAnq1Qv7cvzzHztdsZdAWshXEwvkdclZMXblD2PF7RC-g130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP17166.RAnq1Qv7cvzzHztdsZdAWshXEwvkdclZMXblD2PF7RC-g130_provenance.
- NP17166.RAnq1Qv7cvzzHztdsZdAWshXEwvkdclZMXblD2PF7RC-g130_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." NP17166.RAnq1Qv7cvzzHztdsZdAWshXEwvkdclZMXblD2PF7RC-g130_provenance.
- NP17166.RAnq1Qv7cvzzHztdsZdAWshXEwvkdclZMXblD2PF7RC-g130_assertion evidence source_evidence_curated NP17166.RAnq1Qv7cvzzHztdsZdAWshXEwvkdclZMXblD2PF7RC-g130_provenance.
- NP17166.RAnq1Qv7cvzzHztdsZdAWshXEwvkdclZMXblD2PF7RC-g130_assertion SIO_000772 20711174 NP17166.RAnq1Qv7cvzzHztdsZdAWshXEwvkdclZMXblD2PF7RC-g130_provenance.
- NP17166.RAnq1Qv7cvzzHztdsZdAWshXEwvkdclZMXblD2PF7RC-g130_assertion wasDerivedFrom ctd_human-20150221 NP17166.RAnq1Qv7cvzzHztdsZdAWshXEwvkdclZMXblD2PF7RC-g130_provenance.
- NP17166.RAnq1Qv7cvzzHztdsZdAWshXEwvkdclZMXblD2PF7RC-g130_assertion wasGeneratedBy ECO_0000218 NP17166.RAnq1Qv7cvzzHztdsZdAWshXEwvkdclZMXblD2PF7RC-g130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP17166.RAnq1Qv7cvzzHztdsZdAWshXEwvkdclZMXblD2PF7RC-g130_provenance.