Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP927624.RAACe2j9_pbFtFMJmWF-kgBH9W6JII1CIwyBVUO-uNwOk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP927624.RAACe2j9_pbFtFMJmWF-kgBH9W6JII1CIwyBVUO-uNwOk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP927624.RAACe2j9_pbFtFMJmWF-kgBH9W6JII1CIwyBVUO-uNwOk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP927624.RAACe2j9_pbFtFMJmWF-kgBH9W6JII1CIwyBVUO-uNwOk130_provenance.
- NP927624.RAACe2j9_pbFtFMJmWF-kgBH9W6JII1CIwyBVUO-uNwOk130_assertion description "[Fatal familial insomnia (FFI) is an autosomal dominant prion disease clinically characterized by inattention, sleep loss, dysautonomia, and motor signs and pathologically characterized by a preferential thalamic degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP927624.RAACe2j9_pbFtFMJmWF-kgBH9W6JII1CIwyBVUO-uNwOk130_provenance.
- NP927624.RAACe2j9_pbFtFMJmWF-kgBH9W6JII1CIwyBVUO-uNwOk130_assertion evidence source_evidence_literature NP927624.RAACe2j9_pbFtFMJmWF-kgBH9W6JII1CIwyBVUO-uNwOk130_provenance.
- NP927624.RAACe2j9_pbFtFMJmWF-kgBH9W6JII1CIwyBVUO-uNwOk130_assertion SIO_000772 10389103 NP927624.RAACe2j9_pbFtFMJmWF-kgBH9W6JII1CIwyBVUO-uNwOk130_provenance.
- NP927624.RAACe2j9_pbFtFMJmWF-kgBH9W6JII1CIwyBVUO-uNwOk130_assertion wasDerivedFrom befree-20140225 NP927624.RAACe2j9_pbFtFMJmWF-kgBH9W6JII1CIwyBVUO-uNwOk130_provenance.
- NP927624.RAACe2j9_pbFtFMJmWF-kgBH9W6JII1CIwyBVUO-uNwOk130_assertion wasGeneratedBy ECO_0000203 NP927624.RAACe2j9_pbFtFMJmWF-kgBH9W6JII1CIwyBVUO-uNwOk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP927624.RAACe2j9_pbFtFMJmWF-kgBH9W6JII1CIwyBVUO-uNwOk130_provenance.