Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP422022.RAJ6FQbnPTmKk2XNx1TXYuAVbrhyUCcegyqNYPg75CP1Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP422022.RAJ6FQbnPTmKk2XNx1TXYuAVbrhyUCcegyqNYPg75CP1Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP422022.RAJ6FQbnPTmKk2XNx1TXYuAVbrhyUCcegyqNYPg75CP1Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP422022.RAJ6FQbnPTmKk2XNx1TXYuAVbrhyUCcegyqNYPg75CP1Q130_provenance.
- NP422022.RAJ6FQbnPTmKk2XNx1TXYuAVbrhyUCcegyqNYPg75CP1Q130_assertion description "[Low CSF hypocretin-1 is highly specific (99.1%) and sensitive (88.5%) for narcolepsy with cataplexy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP422022.RAJ6FQbnPTmKk2XNx1TXYuAVbrhyUCcegyqNYPg75CP1Q130_provenance.
- NP422022.RAJ6FQbnPTmKk2XNx1TXYuAVbrhyUCcegyqNYPg75CP1Q130_assertion evidence source_evidence_literature NP422022.RAJ6FQbnPTmKk2XNx1TXYuAVbrhyUCcegyqNYPg75CP1Q130_provenance.
- NP422022.RAJ6FQbnPTmKk2XNx1TXYuAVbrhyUCcegyqNYPg75CP1Q130_assertion SIO_000772 14638887 NP422022.RAJ6FQbnPTmKk2XNx1TXYuAVbrhyUCcegyqNYPg75CP1Q130_provenance.
- NP422022.RAJ6FQbnPTmKk2XNx1TXYuAVbrhyUCcegyqNYPg75CP1Q130_assertion wasDerivedFrom befree-2016 NP422022.RAJ6FQbnPTmKk2XNx1TXYuAVbrhyUCcegyqNYPg75CP1Q130_provenance.
- NP422022.RAJ6FQbnPTmKk2XNx1TXYuAVbrhyUCcegyqNYPg75CP1Q130_assertion wasGeneratedBy ECO_0000203 NP422022.RAJ6FQbnPTmKk2XNx1TXYuAVbrhyUCcegyqNYPg75CP1Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP422022.RAJ6FQbnPTmKk2XNx1TXYuAVbrhyUCcegyqNYPg75CP1Q130_provenance.