Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP927624.RAACe2j9_pbFtFMJmWF-kgBH9W6JII1CIwyBVUO-uNwOk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP927624.RAACe2j9_pbFtFMJmWF-kgBH9W6JII1CIwyBVUO-uNwOk130_assertion type Assertion NP927624.RAACe2j9_pbFtFMJmWF-kgBH9W6JII1CIwyBVUO-uNwOk130_head.
- 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.