Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[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."@en ?g. }

• 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." provenance.
• 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." provenance.
• 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." provenance.
• NP1126909.RAQtUm3B8n2uYTni5wsbKlxLZtT2F8kq6K5b6OTLbZ-pk130_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." NP1126909.RAQtUm3B8n2uYTni5wsbKlxLZtT2F8kq6K5b6OTLbZ-pk130_provenance.
• NP445258.RAjONeViufDeD5kZWC2IeEC8sylvMSUerd8Tim53GfnOU130_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." NP445258.RAjONeViufDeD5kZWC2IeEC8sylvMSUerd8Tim53GfnOU130_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.
• NP445286.RA_AkwdB5bslxIoHpGSSqq57UlRnbMA_vCBQuYj1kPRME130_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." NP445286.RA_AkwdB5bslxIoHpGSSqq57UlRnbMA_vCBQuYj1kPRME130_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.
• 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.