Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP183622.RAEB_DEFm-w9XCrvlEqWLsBx2to9bF1JqYZhCDJPRQfN0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP183622.RAEB_DEFm-w9XCrvlEqWLsBx2to9bF1JqYZhCDJPRQfN0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP183622.RAEB_DEFm-w9XCrvlEqWLsBx2to9bF1JqYZhCDJPRQfN0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP183622.RAEB_DEFm-w9XCrvlEqWLsBx2to9bF1JqYZhCDJPRQfN0130_provenance.
- 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.
- gad-20150221 importedOn "2015-02-21" NP183622.RAEB_DEFm-w9XCrvlEqWLsBx2to9bF1JqYZhCDJPRQfN0130_provenance.