Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1126911.RA5F8FskXrEB1v5uG6Icah64eGMGRwkLaibbKxaEdtT4I130_assertion> ?p ?o ?g. }
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- NP1126911.RA5F8FskXrEB1v5uG6Icah64eGMGRwkLaibbKxaEdtT4I130_assertion type Assertion NP1126911.RA5F8FskXrEB1v5uG6Icah64eGMGRwkLaibbKxaEdtT4I130_head.
- NP1126911.RA5F8FskXrEB1v5uG6Icah64eGMGRwkLaibbKxaEdtT4I130_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." NP1126911.RA5F8FskXrEB1v5uG6Icah64eGMGRwkLaibbKxaEdtT4I130_provenance.
- NP1126911.RA5F8FskXrEB1v5uG6Icah64eGMGRwkLaibbKxaEdtT4I130_assertion evidence source_evidence_literature NP1126911.RA5F8FskXrEB1v5uG6Icah64eGMGRwkLaibbKxaEdtT4I130_provenance.
- NP1126911.RA5F8FskXrEB1v5uG6Icah64eGMGRwkLaibbKxaEdtT4I130_assertion SIO_000772 24215799 NP1126911.RA5F8FskXrEB1v5uG6Icah64eGMGRwkLaibbKxaEdtT4I130_provenance.
- NP1126911.RA5F8FskXrEB1v5uG6Icah64eGMGRwkLaibbKxaEdtT4I130_assertion wasDerivedFrom befree-2016 NP1126911.RA5F8FskXrEB1v5uG6Icah64eGMGRwkLaibbKxaEdtT4I130_provenance.
- NP1126911.RA5F8FskXrEB1v5uG6Icah64eGMGRwkLaibbKxaEdtT4I130_assertion wasGeneratedBy ECO_0000203 NP1126911.RA5F8FskXrEB1v5uG6Icah64eGMGRwkLaibbKxaEdtT4I130_provenance.