Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP970869.RA9ABTgKkIQBFGZi86BF-hpzLiEiahou791BLr22TNOPA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP970869.RA9ABTgKkIQBFGZi86BF-hpzLiEiahou791BLr22TNOPA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP970869.RA9ABTgKkIQBFGZi86BF-hpzLiEiahou791BLr22TNOPA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP970869.RA9ABTgKkIQBFGZi86BF-hpzLiEiahou791BLr22TNOPA130_provenance.
- NP970869.RA9ABTgKkIQBFGZi86BF-hpzLiEiahou791BLr22TNOPA130_assertion description "[Null mutation of the individual OX1R or OX2R in mice substantially ameliorates the narcolepsy/cataplexy phenotype compared to the OX1R/OX2R KO, and highlights specific roles of the individual receptors in sleep architecture, the OX1R KO demonstrating an a attenuated sleep phenotype relative to the OX2R KO.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP970869.RA9ABTgKkIQBFGZi86BF-hpzLiEiahou791BLr22TNOPA130_provenance.
- NP970869.RA9ABTgKkIQBFGZi86BF-hpzLiEiahou791BLr22TNOPA130_assertion evidence source_evidence_literature NP970869.RA9ABTgKkIQBFGZi86BF-hpzLiEiahou791BLr22TNOPA130_provenance.
- NP970869.RA9ABTgKkIQBFGZi86BF-hpzLiEiahou791BLr22TNOPA130_assertion SIO_000772 24215799 NP970869.RA9ABTgKkIQBFGZi86BF-hpzLiEiahou791BLr22TNOPA130_provenance.
- NP970869.RA9ABTgKkIQBFGZi86BF-hpzLiEiahou791BLr22TNOPA130_assertion wasDerivedFrom befree-20150227 NP970869.RA9ABTgKkIQBFGZi86BF-hpzLiEiahou791BLr22TNOPA130_provenance.
- NP970869.RA9ABTgKkIQBFGZi86BF-hpzLiEiahou791BLr22TNOPA130_assertion wasGeneratedBy ECO_0000203 NP970869.RA9ABTgKkIQBFGZi86BF-hpzLiEiahou791BLr22TNOPA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP970869.RA9ABTgKkIQBFGZi86BF-hpzLiEiahou791BLr22TNOPA130_provenance.