Matches in Nanopublications for { ?s ?p "[The orexin-2/hypocretin-2 (OX2R) receptor gene is mutated in canine narcolepsy and disruption of the prepro-orexin/hypocretin ligand gene results in both an animal model of narcolepsy and sporadic cases of the human disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP453313.RABBOwhweJk16UmrZgCBSP2kCzZ9hBzq2diLY--P41zJQ130_assertion description "[The orexin-2/hypocretin-2 (OX2R) receptor gene is mutated in canine narcolepsy and disruption of the prepro-orexin/hypocretin ligand gene results in both an animal model of narcolepsy and sporadic cases of the human disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP453313.RABBOwhweJk16UmrZgCBSP2kCzZ9hBzq2diLY--P41zJQ130_provenance.
- NP453316.RAP3WWN93o3eQ0zIhrJVzwKJgGGQcnjTtfOW6qFm9bRds130_assertion description "[The orexin-2/hypocretin-2 (OX2R) receptor gene is mutated in canine narcolepsy and disruption of the prepro-orexin/hypocretin ligand gene results in both an animal model of narcolepsy and sporadic cases of the human disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP453316.RAP3WWN93o3eQ0zIhrJVzwKJgGGQcnjTtfOW6qFm9bRds130_provenance.
- NP453314.RArG97WfTtJInLeq-7cv3TUoNtcyCJrMgn-NI1sDhnjmg130_assertion description "[The orexin-2/hypocretin-2 (OX2R) receptor gene is mutated in canine narcolepsy and disruption of the prepro-orexin/hypocretin ligand gene results in both an animal model of narcolepsy and sporadic cases of the human disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP453314.RArG97WfTtJInLeq-7cv3TUoNtcyCJrMgn-NI1sDhnjmg130_provenance.