Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1126914.RAoPfdBE_9Ve2b5IkaOg92boBbQTQX6_-i44uhQ8J2tN4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1126914.RAoPfdBE_9Ve2b5IkaOg92boBbQTQX6_-i44uhQ8J2tN4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1126914.RAoPfdBE_9Ve2b5IkaOg92boBbQTQX6_-i44uhQ8J2tN4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1126914.RAoPfdBE_9Ve2b5IkaOg92boBbQTQX6_-i44uhQ8J2tN4130_provenance.
- NP1126914.RAoPfdBE_9Ve2b5IkaOg92boBbQTQX6_-i44uhQ8J2tN4130_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." NP1126914.RAoPfdBE_9Ve2b5IkaOg92boBbQTQX6_-i44uhQ8J2tN4130_provenance.
- NP1126914.RAoPfdBE_9Ve2b5IkaOg92boBbQTQX6_-i44uhQ8J2tN4130_assertion evidence source_evidence_literature NP1126914.RAoPfdBE_9Ve2b5IkaOg92boBbQTQX6_-i44uhQ8J2tN4130_provenance.
- NP1126914.RAoPfdBE_9Ve2b5IkaOg92boBbQTQX6_-i44uhQ8J2tN4130_assertion SIO_000772 24215799 NP1126914.RAoPfdBE_9Ve2b5IkaOg92boBbQTQX6_-i44uhQ8J2tN4130_provenance.
- NP1126914.RAoPfdBE_9Ve2b5IkaOg92boBbQTQX6_-i44uhQ8J2tN4130_assertion wasDerivedFrom befree-2016 NP1126914.RAoPfdBE_9Ve2b5IkaOg92boBbQTQX6_-i44uhQ8J2tN4130_provenance.
- NP1126914.RAoPfdBE_9Ve2b5IkaOg92boBbQTQX6_-i44uhQ8J2tN4130_assertion wasGeneratedBy ECO_0000203 NP1126914.RAoPfdBE_9Ve2b5IkaOg92boBbQTQX6_-i44uhQ8J2tN4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1126914.RAoPfdBE_9Ve2b5IkaOg92boBbQTQX6_-i44uhQ8J2tN4130_provenance.