Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP384499.RAG3y29RA3fDAV7nZVOHU2QQvTEgZIdKIpQpQ5LvCzAus130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP384499.RAG3y29RA3fDAV7nZVOHU2QQvTEgZIdKIpQpQ5LvCzAus130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP384499.RAG3y29RA3fDAV7nZVOHU2QQvTEgZIdKIpQpQ5LvCzAus130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP384499.RAG3y29RA3fDAV7nZVOHU2QQvTEgZIdKIpQpQ5LvCzAus130_provenance.
- NP384499.RAG3y29RA3fDAV7nZVOHU2QQvTEgZIdKIpQpQ5LvCzAus130_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." NP384499.RAG3y29RA3fDAV7nZVOHU2QQvTEgZIdKIpQpQ5LvCzAus130_provenance.
- NP384499.RAG3y29RA3fDAV7nZVOHU2QQvTEgZIdKIpQpQ5LvCzAus130_assertion evidence source_evidence_literature NP384499.RAG3y29RA3fDAV7nZVOHU2QQvTEgZIdKIpQpQ5LvCzAus130_provenance.
- NP384499.RAG3y29RA3fDAV7nZVOHU2QQvTEgZIdKIpQpQ5LvCzAus130_assertion SIO_000772 10389103 NP384499.RAG3y29RA3fDAV7nZVOHU2QQvTEgZIdKIpQpQ5LvCzAus130_provenance.
- NP384499.RAG3y29RA3fDAV7nZVOHU2QQvTEgZIdKIpQpQ5LvCzAus130_assertion wasDerivedFrom befree-20140225 NP384499.RAG3y29RA3fDAV7nZVOHU2QQvTEgZIdKIpQpQ5LvCzAus130_provenance.
- NP384499.RAG3y29RA3fDAV7nZVOHU2QQvTEgZIdKIpQpQ5LvCzAus130_assertion wasGeneratedBy ECO_0000203 NP384499.RAG3y29RA3fDAV7nZVOHU2QQvTEgZIdKIpQpQ5LvCzAus130_provenance.
- befree-20140225 importedOn "2014-02-25" NP384499.RAG3y29RA3fDAV7nZVOHU2QQvTEgZIdKIpQpQ5LvCzAus130_provenance.