Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP865084.RA5JQ28XIz6Px5fnQ3RDRH8e9Bf-sAI182TXwlw0P_3xU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP865084.RA5JQ28XIz6Px5fnQ3RDRH8e9Bf-sAI182TXwlw0P_3xU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP865084.RA5JQ28XIz6Px5fnQ3RDRH8e9Bf-sAI182TXwlw0P_3xU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP865084.RA5JQ28XIz6Px5fnQ3RDRH8e9Bf-sAI182TXwlw0P_3xU130_provenance.
- NP865084.RA5JQ28XIz6Px5fnQ3RDRH8e9Bf-sAI182TXwlw0P_3xU130_assertion description "[CSF hypocretin-1 was measured by a sensitive radioimmunoassay in 47 patients with narcolepsy with cataplexy, 7 with narcolepsy without cataplexy, 10 with idiopathic CNS hypersomnia, and a control group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP865084.RA5JQ28XIz6Px5fnQ3RDRH8e9Bf-sAI182TXwlw0P_3xU130_provenance.
- NP865084.RA5JQ28XIz6Px5fnQ3RDRH8e9Bf-sAI182TXwlw0P_3xU130_assertion evidence source_evidence_literature NP865084.RA5JQ28XIz6Px5fnQ3RDRH8e9Bf-sAI182TXwlw0P_3xU130_provenance.
- NP865084.RA5JQ28XIz6Px5fnQ3RDRH8e9Bf-sAI182TXwlw0P_3xU130_assertion SIO_000772 17702265 NP865084.RA5JQ28XIz6Px5fnQ3RDRH8e9Bf-sAI182TXwlw0P_3xU130_provenance.
- NP865084.RA5JQ28XIz6Px5fnQ3RDRH8e9Bf-sAI182TXwlw0P_3xU130_assertion wasDerivedFrom befree-20140225 NP865084.RA5JQ28XIz6Px5fnQ3RDRH8e9Bf-sAI182TXwlw0P_3xU130_provenance.
- NP865084.RA5JQ28XIz6Px5fnQ3RDRH8e9Bf-sAI182TXwlw0P_3xU130_assertion wasGeneratedBy ECO_0000203 NP865084.RA5JQ28XIz6Px5fnQ3RDRH8e9Bf-sAI182TXwlw0P_3xU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP865084.RA5JQ28XIz6Px5fnQ3RDRH8e9Bf-sAI182TXwlw0P_3xU130_provenance.