Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP795192.RACWsSOq-qNzYeUN3AIMIS2EnSfPzNBVi5Nr5Jto5ipnE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP795192.RACWsSOq-qNzYeUN3AIMIS2EnSfPzNBVi5Nr5Jto5ipnE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP795192.RACWsSOq-qNzYeUN3AIMIS2EnSfPzNBVi5Nr5Jto5ipnE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP795192.RACWsSOq-qNzYeUN3AIMIS2EnSfPzNBVi5Nr5Jto5ipnE130_provenance.
- NP795192.RACWsSOq-qNzYeUN3AIMIS2EnSfPzNBVi5Nr5Jto5ipnE130_assertion description "[Interviews, polysomnography, multiple sleep latency test, HLA-typing, and CSF hcrt-1 measurements in Danish patients with narcolepsy with cataplexy (NC) and narcolepsy without cataplexy (NwC), CSF hcrt-1 measurements in other hypersomnias, neurological and normal controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP795192.RACWsSOq-qNzYeUN3AIMIS2EnSfPzNBVi5Nr5Jto5ipnE130_provenance.
- NP795192.RACWsSOq-qNzYeUN3AIMIS2EnSfPzNBVi5Nr5Jto5ipnE130_assertion evidence source_evidence_literature NP795192.RACWsSOq-qNzYeUN3AIMIS2EnSfPzNBVi5Nr5Jto5ipnE130_provenance.
- NP795192.RACWsSOq-qNzYeUN3AIMIS2EnSfPzNBVi5Nr5Jto5ipnE130_assertion SIO_000772 20175400 NP795192.RACWsSOq-qNzYeUN3AIMIS2EnSfPzNBVi5Nr5Jto5ipnE130_provenance.
- NP795192.RACWsSOq-qNzYeUN3AIMIS2EnSfPzNBVi5Nr5Jto5ipnE130_assertion wasDerivedFrom befree-2016 NP795192.RACWsSOq-qNzYeUN3AIMIS2EnSfPzNBVi5Nr5Jto5ipnE130_provenance.
- NP795192.RACWsSOq-qNzYeUN3AIMIS2EnSfPzNBVi5Nr5Jto5ipnE130_assertion wasGeneratedBy ECO_0000203 NP795192.RACWsSOq-qNzYeUN3AIMIS2EnSfPzNBVi5Nr5Jto5ipnE130_provenance.
- befree-2016 importedOn "2016-02-19" NP795192.RACWsSOq-qNzYeUN3AIMIS2EnSfPzNBVi5Nr5Jto5ipnE130_provenance.