Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP445193.RA9VC7XQe9mf2Sgi7E_QfNoRVcort0rEJH-QRJhSEIUX4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP445193.RA9VC7XQe9mf2Sgi7E_QfNoRVcort0rEJH-QRJhSEIUX4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP445193.RA9VC7XQe9mf2Sgi7E_QfNoRVcort0rEJH-QRJhSEIUX4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP445193.RA9VC7XQe9mf2Sgi7E_QfNoRVcort0rEJH-QRJhSEIUX4130_provenance.
- NP445193.RA9VC7XQe9mf2Sgi7E_QfNoRVcort0rEJH-QRJhSEIUX4130_assertion description "[(1) Hypocretin dysfunction is not the 'final common pathway' in the pathophysiology of most hypersomnolent syndromes that fall on the borderline for a diagnosis of narcolepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP445193.RA9VC7XQe9mf2Sgi7E_QfNoRVcort0rEJH-QRJhSEIUX4130_provenance.
- NP445193.RA9VC7XQe9mf2Sgi7E_QfNoRVcort0rEJH-QRJhSEIUX4130_assertion evidence source_evidence_literature NP445193.RA9VC7XQe9mf2Sgi7E_QfNoRVcort0rEJH-QRJhSEIUX4130_provenance.
- NP445193.RA9VC7XQe9mf2Sgi7E_QfNoRVcort0rEJH-QRJhSEIUX4130_assertion SIO_000772 14592354 NP445193.RA9VC7XQe9mf2Sgi7E_QfNoRVcort0rEJH-QRJhSEIUX4130_provenance.
- NP445193.RA9VC7XQe9mf2Sgi7E_QfNoRVcort0rEJH-QRJhSEIUX4130_assertion wasDerivedFrom befree-20150227 NP445193.RA9VC7XQe9mf2Sgi7E_QfNoRVcort0rEJH-QRJhSEIUX4130_provenance.
- NP445193.RA9VC7XQe9mf2Sgi7E_QfNoRVcort0rEJH-QRJhSEIUX4130_assertion wasGeneratedBy ECO_0000203 NP445193.RA9VC7XQe9mf2Sgi7E_QfNoRVcort0rEJH-QRJhSEIUX4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP445193.RA9VC7XQe9mf2Sgi7E_QfNoRVcort0rEJH-QRJhSEIUX4130_provenance.