Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP795187.RARxJUvcwjNy_Ab_a75CDAABd5D2UIqAp3BmyR_B_5E50130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP795187.RARxJUvcwjNy_Ab_a75CDAABd5D2UIqAp3BmyR_B_5E50130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP795187.RARxJUvcwjNy_Ab_a75CDAABd5D2UIqAp3BmyR_B_5E50130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP795187.RARxJUvcwjNy_Ab_a75CDAABd5D2UIqAp3BmyR_B_5E50130_provenance.
- NP795187.RARxJUvcwjNy_Ab_a75CDAABd5D2UIqAp3BmyR_B_5E50130_assertion description "[The ICSD-2 criterion for low CSF hcrt-1 (< 30% of normal mean) is valid for diagnosing NC, but not NwC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP795187.RARxJUvcwjNy_Ab_a75CDAABd5D2UIqAp3BmyR_B_5E50130_provenance.
- NP795187.RARxJUvcwjNy_Ab_a75CDAABd5D2UIqAp3BmyR_B_5E50130_assertion evidence source_evidence_literature NP795187.RARxJUvcwjNy_Ab_a75CDAABd5D2UIqAp3BmyR_B_5E50130_provenance.
- NP795187.RARxJUvcwjNy_Ab_a75CDAABd5D2UIqAp3BmyR_B_5E50130_assertion SIO_000772 20175400 NP795187.RARxJUvcwjNy_Ab_a75CDAABd5D2UIqAp3BmyR_B_5E50130_provenance.
- NP795187.RARxJUvcwjNy_Ab_a75CDAABd5D2UIqAp3BmyR_B_5E50130_assertion wasDerivedFrom befree-2016 NP795187.RARxJUvcwjNy_Ab_a75CDAABd5D2UIqAp3BmyR_B_5E50130_provenance.
- NP795187.RARxJUvcwjNy_Ab_a75CDAABd5D2UIqAp3BmyR_B_5E50130_assertion wasGeneratedBy ECO_0000203 NP795187.RARxJUvcwjNy_Ab_a75CDAABd5D2UIqAp3BmyR_B_5E50130_provenance.
- befree-2016 importedOn "2016-02-19" NP795187.RARxJUvcwjNy_Ab_a75CDAABd5D2UIqAp3BmyR_B_5E50130_provenance.