Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP17166.RAnq1Qv7cvzzHztdsZdAWshXEwvkdclZMXblD2PF7RC-g130_assertion> ?p ?o ?g. }
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- NP17166.RAnq1Qv7cvzzHztdsZdAWshXEwvkdclZMXblD2PF7RC-g130_assertion type Assertion NP17166.RAnq1Qv7cvzzHztdsZdAWshXEwvkdclZMXblD2PF7RC-g130_head.
- 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.