Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP323196.RAgf-lCSpXwZjo4gU0YZ5-FwtjFRjhnkPh313szMtgAHw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP323196.RAgf-lCSpXwZjo4gU0YZ5-FwtjFRjhnkPh313szMtgAHw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP323196.RAgf-lCSpXwZjo4gU0YZ5-FwtjFRjhnkPh313szMtgAHw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP323196.RAgf-lCSpXwZjo4gU0YZ5-FwtjFRjhnkPh313szMtgAHw130_provenance.
- NP323196.RAgf-lCSpXwZjo4gU0YZ5-FwtjFRjhnkPh313szMtgAHw130_assertion description "[We investigated polymorphisms of MAO-A and catechol-O-methyltransferase (COMT) in 97 Caucasians with well-defined narcolepsy-cataplexy and sought for genotypic effects on disease symptoms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323196.RAgf-lCSpXwZjo4gU0YZ5-FwtjFRjhnkPh313szMtgAHw130_provenance.
- NP323196.RAgf-lCSpXwZjo4gU0YZ5-FwtjFRjhnkPh313szMtgAHw130_assertion evidence source_evidence_literature NP323196.RAgf-lCSpXwZjo4gU0YZ5-FwtjFRjhnkPh313szMtgAHw130_provenance.
- NP323196.RAgf-lCSpXwZjo4gU0YZ5-FwtjFRjhnkPh313szMtgAHw130_assertion SIO_000772 11443519 NP323196.RAgf-lCSpXwZjo4gU0YZ5-FwtjFRjhnkPh313szMtgAHw130_provenance.
- NP323196.RAgf-lCSpXwZjo4gU0YZ5-FwtjFRjhnkPh313szMtgAHw130_assertion wasDerivedFrom befree-2016 NP323196.RAgf-lCSpXwZjo4gU0YZ5-FwtjFRjhnkPh313szMtgAHw130_provenance.
- NP323196.RAgf-lCSpXwZjo4gU0YZ5-FwtjFRjhnkPh313szMtgAHw130_assertion wasGeneratedBy ECO_0000203 NP323196.RAgf-lCSpXwZjo4gU0YZ5-FwtjFRjhnkPh313szMtgAHw130_provenance.
- befree-2016 importedOn "2016-02-19" NP323196.RAgf-lCSpXwZjo4gU0YZ5-FwtjFRjhnkPh313szMtgAHw130_provenance.