Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP183622.RAEB_DEFm-w9XCrvlEqWLsBx2to9bF1JqYZhCDJPRQfN0130_assertion> ?p ?o ?g. }
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- NP183622.RAEB_DEFm-w9XCrvlEqWLsBx2to9bF1JqYZhCDJPRQfN0130_assertion type Assertion NP183622.RAEB_DEFm-w9XCrvlEqWLsBx2to9bF1JqYZhCDJPRQfN0130_head.
- NP183622.RAEB_DEFm-w9XCrvlEqWLsBx2to9bF1JqYZhCDJPRQfN0130_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." NP183622.RAEB_DEFm-w9XCrvlEqWLsBx2to9bF1JqYZhCDJPRQfN0130_provenance.
- NP183622.RAEB_DEFm-w9XCrvlEqWLsBx2to9bF1JqYZhCDJPRQfN0130_assertion evidence source_evidence_literature NP183622.RAEB_DEFm-w9XCrvlEqWLsBx2to9bF1JqYZhCDJPRQfN0130_provenance.
- NP183622.RAEB_DEFm-w9XCrvlEqWLsBx2to9bF1JqYZhCDJPRQfN0130_assertion SIO_000772 20711174 NP183622.RAEB_DEFm-w9XCrvlEqWLsBx2to9bF1JqYZhCDJPRQfN0130_provenance.
- NP183622.RAEB_DEFm-w9XCrvlEqWLsBx2to9bF1JqYZhCDJPRQfN0130_assertion wasDerivedFrom gad-20150221 NP183622.RAEB_DEFm-w9XCrvlEqWLsBx2to9bF1JqYZhCDJPRQfN0130_provenance.
- NP183622.RAEB_DEFm-w9XCrvlEqWLsBx2to9bF1JqYZhCDJPRQfN0130_assertion wasGeneratedBy ECO_0000203 NP183622.RAEB_DEFm-w9XCrvlEqWLsBx2to9bF1JqYZhCDJPRQfN0130_provenance.