Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP216670.RAOAd1GyLilKFZDe95rxw6Dp-L9akMFVMle_dhf02LcUk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP216670.RAOAd1GyLilKFZDe95rxw6Dp-L9akMFVMle_dhf02LcUk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP216670.RAOAd1GyLilKFZDe95rxw6Dp-L9akMFVMle_dhf02LcUk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP216670.RAOAd1GyLilKFZDe95rxw6Dp-L9akMFVMle_dhf02LcUk130_provenance.
- NP216670.RAOAd1GyLilKFZDe95rxw6Dp-L9akMFVMle_dhf02LcUk130_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." NP216670.RAOAd1GyLilKFZDe95rxw6Dp-L9akMFVMle_dhf02LcUk130_provenance.
- NP216670.RAOAd1GyLilKFZDe95rxw6Dp-L9akMFVMle_dhf02LcUk130_assertion evidence source_evidence_literature NP216670.RAOAd1GyLilKFZDe95rxw6Dp-L9akMFVMle_dhf02LcUk130_provenance.
- NP216670.RAOAd1GyLilKFZDe95rxw6Dp-L9akMFVMle_dhf02LcUk130_assertion SIO_000772 14638887 NP216670.RAOAd1GyLilKFZDe95rxw6Dp-L9akMFVMle_dhf02LcUk130_provenance.
- NP216670.RAOAd1GyLilKFZDe95rxw6Dp-L9akMFVMle_dhf02LcUk130_assertion wasDerivedFrom befree-20140225 NP216670.RAOAd1GyLilKFZDe95rxw6Dp-L9akMFVMle_dhf02LcUk130_provenance.
- NP216670.RAOAd1GyLilKFZDe95rxw6Dp-L9akMFVMle_dhf02LcUk130_assertion wasGeneratedBy ECO_0000203 NP216670.RAOAd1GyLilKFZDe95rxw6Dp-L9akMFVMle_dhf02LcUk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP216670.RAOAd1GyLilKFZDe95rxw6Dp-L9akMFVMle_dhf02LcUk130_provenance.