Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP453314.RArG97WfTtJInLeq-7cv3TUoNtcyCJrMgn-NI1sDhnjmg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP453314.RArG97WfTtJInLeq-7cv3TUoNtcyCJrMgn-NI1sDhnjmg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP453314.RArG97WfTtJInLeq-7cv3TUoNtcyCJrMgn-NI1sDhnjmg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP453314.RArG97WfTtJInLeq-7cv3TUoNtcyCJrMgn-NI1sDhnjmg130_provenance.
- befree-2016 importedOn "2016-02-19" NP453314.RArG97WfTtJInLeq-7cv3TUoNtcyCJrMgn-NI1sDhnjmg130_provenance.
- NP453314.RArG97WfTtJInLeq-7cv3TUoNtcyCJrMgn-NI1sDhnjmg130_assertion wasGeneratedBy ECO_0000203 NP453314.RArG97WfTtJInLeq-7cv3TUoNtcyCJrMgn-NI1sDhnjmg130_provenance.
- NP453314.RArG97WfTtJInLeq-7cv3TUoNtcyCJrMgn-NI1sDhnjmg130_assertion wasDerivedFrom befree-2016 NP453314.RArG97WfTtJInLeq-7cv3TUoNtcyCJrMgn-NI1sDhnjmg130_provenance.
- NP453314.RArG97WfTtJInLeq-7cv3TUoNtcyCJrMgn-NI1sDhnjmg130_assertion SIO_000772 15274044 NP453314.RArG97WfTtJInLeq-7cv3TUoNtcyCJrMgn-NI1sDhnjmg130_provenance.
- NP453314.RArG97WfTtJInLeq-7cv3TUoNtcyCJrMgn-NI1sDhnjmg130_assertion evidence source_evidence_literature NP453314.RArG97WfTtJInLeq-7cv3TUoNtcyCJrMgn-NI1sDhnjmg130_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.