Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP306877.RA7loZ0q2h90G4XGWgYQvH1N7p8gLH363aYiTtYOrNtZY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP306877.RA7loZ0q2h90G4XGWgYQvH1N7p8gLH363aYiTtYOrNtZY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP306877.RA7loZ0q2h90G4XGWgYQvH1N7p8gLH363aYiTtYOrNtZY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP306877.RA7loZ0q2h90G4XGWgYQvH1N7p8gLH363aYiTtYOrNtZY130_provenance.
- NP306877.RA7loZ0q2h90G4XGWgYQvH1N7p8gLH363aYiTtYOrNtZY130_assertion description "[SCA-12 is a slowly progressive, autosomal dominant, neurodegenerative disorder that differs from other SCA in that it typically presents with action tremor in patients in their mid 30s and usually includes hyperreflexia and subtle parkinsonian signs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP306877.RA7loZ0q2h90G4XGWgYQvH1N7p8gLH363aYiTtYOrNtZY130_provenance.
- NP306877.RA7loZ0q2h90G4XGWgYQvH1N7p8gLH363aYiTtYOrNtZY130_assertion evidence source_evidence_literature NP306877.RA7loZ0q2h90G4XGWgYQvH1N7p8gLH363aYiTtYOrNtZY130_provenance.
- NP306877.RA7loZ0q2h90G4XGWgYQvH1N7p8gLH363aYiTtYOrNtZY130_assertion SIO_000772 11171892 NP306877.RA7loZ0q2h90G4XGWgYQvH1N7p8gLH363aYiTtYOrNtZY130_provenance.
- NP306877.RA7loZ0q2h90G4XGWgYQvH1N7p8gLH363aYiTtYOrNtZY130_assertion wasDerivedFrom befree-2016 NP306877.RA7loZ0q2h90G4XGWgYQvH1N7p8gLH363aYiTtYOrNtZY130_provenance.
- NP306877.RA7loZ0q2h90G4XGWgYQvH1N7p8gLH363aYiTtYOrNtZY130_assertion wasGeneratedBy ECO_0000203 NP306877.RA7loZ0q2h90G4XGWgYQvH1N7p8gLH363aYiTtYOrNtZY130_provenance.
- befree-2016 importedOn "2016-02-19" NP306877.RA7loZ0q2h90G4XGWgYQvH1N7p8gLH363aYiTtYOrNtZY130_provenance.