Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418370.RAo5IVciRxvyIMrrhQnoLPReukrA7pssBefYtz29rEsv4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418370.RAo5IVciRxvyIMrrhQnoLPReukrA7pssBefYtz29rEsv4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418370.RAo5IVciRxvyIMrrhQnoLPReukrA7pssBefYtz29rEsv4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418370.RAo5IVciRxvyIMrrhQnoLPReukrA7pssBefYtz29rEsv4130_provenance.
- NP418370.RAo5IVciRxvyIMrrhQnoLPReukrA7pssBefYtz29rEsv4130_assertion description "[After the discovery of the type 2 hypocretin receptor mutation in canine narcolepsy and the finding of a CSF hypocretin-1 deficiency in human narcolepsy, the major stream of research has involved the hypocretinergic system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418370.RAo5IVciRxvyIMrrhQnoLPReukrA7pssBefYtz29rEsv4130_provenance.
- NP418370.RAo5IVciRxvyIMrrhQnoLPReukrA7pssBefYtz29rEsv4130_assertion evidence source_evidence_literature NP418370.RAo5IVciRxvyIMrrhQnoLPReukrA7pssBefYtz29rEsv4130_provenance.
- NP418370.RAo5IVciRxvyIMrrhQnoLPReukrA7pssBefYtz29rEsv4130_assertion SIO_000772 14580598 NP418370.RAo5IVciRxvyIMrrhQnoLPReukrA7pssBefYtz29rEsv4130_provenance.
- NP418370.RAo5IVciRxvyIMrrhQnoLPReukrA7pssBefYtz29rEsv4130_assertion wasDerivedFrom befree-2016 NP418370.RAo5IVciRxvyIMrrhQnoLPReukrA7pssBefYtz29rEsv4130_provenance.
- NP418370.RAo5IVciRxvyIMrrhQnoLPReukrA7pssBefYtz29rEsv4130_assertion wasGeneratedBy ECO_0000203 NP418370.RAo5IVciRxvyIMrrhQnoLPReukrA7pssBefYtz29rEsv4130_provenance.
- befree-2016 importedOn "2016-02-19" NP418370.RAo5IVciRxvyIMrrhQnoLPReukrA7pssBefYtz29rEsv4130_provenance.