Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP531231.RAZ4iKs1YYYDgvFCoxQ3Ne-XkFi-Iy44mU0vTLQgp7SdI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP531231.RAZ4iKs1YYYDgvFCoxQ3Ne-XkFi-Iy44mU0vTLQgp7SdI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP531231.RAZ4iKs1YYYDgvFCoxQ3Ne-XkFi-Iy44mU0vTLQgp7SdI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP531231.RAZ4iKs1YYYDgvFCoxQ3Ne-XkFi-Iy44mU0vTLQgp7SdI130_provenance.
- NP531231.RAZ4iKs1YYYDgvFCoxQ3Ne-XkFi-Iy44mU0vTLQgp7SdI130_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." NP531231.RAZ4iKs1YYYDgvFCoxQ3Ne-XkFi-Iy44mU0vTLQgp7SdI130_provenance.
- NP531231.RAZ4iKs1YYYDgvFCoxQ3Ne-XkFi-Iy44mU0vTLQgp7SdI130_assertion evidence source_evidence_literature NP531231.RAZ4iKs1YYYDgvFCoxQ3Ne-XkFi-Iy44mU0vTLQgp7SdI130_provenance.
- NP531231.RAZ4iKs1YYYDgvFCoxQ3Ne-XkFi-Iy44mU0vTLQgp7SdI130_assertion SIO_000772 14638887 NP531231.RAZ4iKs1YYYDgvFCoxQ3Ne-XkFi-Iy44mU0vTLQgp7SdI130_provenance.
- NP531231.RAZ4iKs1YYYDgvFCoxQ3Ne-XkFi-Iy44mU0vTLQgp7SdI130_assertion wasDerivedFrom befree-20150227 NP531231.RAZ4iKs1YYYDgvFCoxQ3Ne-XkFi-Iy44mU0vTLQgp7SdI130_provenance.
- NP531231.RAZ4iKs1YYYDgvFCoxQ3Ne-XkFi-Iy44mU0vTLQgp7SdI130_assertion wasGeneratedBy ECO_0000203 NP531231.RAZ4iKs1YYYDgvFCoxQ3Ne-XkFi-Iy44mU0vTLQgp7SdI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP531231.RAZ4iKs1YYYDgvFCoxQ3Ne-XkFi-Iy44mU0vTLQgp7SdI130_provenance.