Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP404978.RA9PWlsIem8ZqvXZwWD4EfOekMwl8l5GqRI1D13651wAk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP404978.RA9PWlsIem8ZqvXZwWD4EfOekMwl8l5GqRI1D13651wAk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP404978.RA9PWlsIem8ZqvXZwWD4EfOekMwl8l5GqRI1D13651wAk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP404978.RA9PWlsIem8ZqvXZwWD4EfOekMwl8l5GqRI1D13651wAk130_provenance.
- NP404978.RA9PWlsIem8ZqvXZwWD4EfOekMwl8l5GqRI1D13651wAk130_assertion description "[We recently reported a novel -62�G/A polymorphism within ataxin 8 (ATXN8) gene promoter region, with -62�G displaying significantly higher luciferase activity compared with -62 A. Phenotypic variability in spinocerebellar ataxia type 8 (SCA8) has been suggested, and large SCA8 repeats were found in patients with Parkinson's disease (PD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404978.RA9PWlsIem8ZqvXZwWD4EfOekMwl8l5GqRI1D13651wAk130_provenance.
- NP404978.RA9PWlsIem8ZqvXZwWD4EfOekMwl8l5GqRI1D13651wAk130_assertion evidence source_evidence_literature NP404978.RA9PWlsIem8ZqvXZwWD4EfOekMwl8l5GqRI1D13651wAk130_provenance.
- NP404978.RA9PWlsIem8ZqvXZwWD4EfOekMwl8l5GqRI1D13651wAk130_assertion SIO_000772 22577844 NP404978.RA9PWlsIem8ZqvXZwWD4EfOekMwl8l5GqRI1D13651wAk130_provenance.
- NP404978.RA9PWlsIem8ZqvXZwWD4EfOekMwl8l5GqRI1D13651wAk130_assertion wasDerivedFrom befree-20140225 NP404978.RA9PWlsIem8ZqvXZwWD4EfOekMwl8l5GqRI1D13651wAk130_provenance.
- NP404978.RA9PWlsIem8ZqvXZwWD4EfOekMwl8l5GqRI1D13651wAk130_assertion wasGeneratedBy ECO_0000203 NP404978.RA9PWlsIem8ZqvXZwWD4EfOekMwl8l5GqRI1D13651wAk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP404978.RA9PWlsIem8ZqvXZwWD4EfOekMwl8l5GqRI1D13651wAk130_provenance.