Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP220508.RAAqmfnD1ZPsgUo9vztlwYwZoR9nh1WOZ1y7nrNC2ni_8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP220508.RAAqmfnD1ZPsgUo9vztlwYwZoR9nh1WOZ1y7nrNC2ni_8130_assertion type Assertion NP220508.RAAqmfnD1ZPsgUo9vztlwYwZoR9nh1WOZ1y7nrNC2ni_8130_head.
- NP220508.RAAqmfnD1ZPsgUo9vztlwYwZoR9nh1WOZ1y7nrNC2ni_8130_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." NP220508.RAAqmfnD1ZPsgUo9vztlwYwZoR9nh1WOZ1y7nrNC2ni_8130_provenance.
- NP220508.RAAqmfnD1ZPsgUo9vztlwYwZoR9nh1WOZ1y7nrNC2ni_8130_assertion evidence source_evidence_literature NP220508.RAAqmfnD1ZPsgUo9vztlwYwZoR9nh1WOZ1y7nrNC2ni_8130_provenance.
- NP220508.RAAqmfnD1ZPsgUo9vztlwYwZoR9nh1WOZ1y7nrNC2ni_8130_assertion SIO_000772 20711174 NP220508.RAAqmfnD1ZPsgUo9vztlwYwZoR9nh1WOZ1y7nrNC2ni_8130_provenance.
- NP220508.RAAqmfnD1ZPsgUo9vztlwYwZoR9nh1WOZ1y7nrNC2ni_8130_assertion wasDerivedFrom befree-20140225 NP220508.RAAqmfnD1ZPsgUo9vztlwYwZoR9nh1WOZ1y7nrNC2ni_8130_provenance.
- NP220508.RAAqmfnD1ZPsgUo9vztlwYwZoR9nh1WOZ1y7nrNC2ni_8130_assertion wasGeneratedBy ECO_0000203 NP220508.RAAqmfnD1ZPsgUo9vztlwYwZoR9nh1WOZ1y7nrNC2ni_8130_provenance.