Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP681692.RA-vJI5kyJeuxRdzHJ4bIjhnLhudLmW29mRtT_gcUZELU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP681692.RA-vJI5kyJeuxRdzHJ4bIjhnLhudLmW29mRtT_gcUZELU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP681692.RA-vJI5kyJeuxRdzHJ4bIjhnLhudLmW29mRtT_gcUZELU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP681692.RA-vJI5kyJeuxRdzHJ4bIjhnLhudLmW29mRtT_gcUZELU130_provenance.
- NP681692.RA-vJI5kyJeuxRdzHJ4bIjhnLhudLmW29mRtT_gcUZELU130_assertion description "[Progression was faster in patients with SCA2 mutations and normal alleles with 22 or fewer repeats (P = .02) and in patients with SCA3 mutations with parkinsonism and/or dystonia at baseline (P = .003).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681692.RA-vJI5kyJeuxRdzHJ4bIjhnLhudLmW29mRtT_gcUZELU130_provenance.
- NP681692.RA-vJI5kyJeuxRdzHJ4bIjhnLhudLmW29mRtT_gcUZELU130_assertion evidence source_evidence_literature NP681692.RA-vJI5kyJeuxRdzHJ4bIjhnLhudLmW29mRtT_gcUZELU130_provenance.
- NP681692.RA-vJI5kyJeuxRdzHJ4bIjhnLhudLmW29mRtT_gcUZELU130_assertion SIO_000772 22491195 NP681692.RA-vJI5kyJeuxRdzHJ4bIjhnLhudLmW29mRtT_gcUZELU130_provenance.
- NP681692.RA-vJI5kyJeuxRdzHJ4bIjhnLhudLmW29mRtT_gcUZELU130_assertion wasDerivedFrom befree-20150227 NP681692.RA-vJI5kyJeuxRdzHJ4bIjhnLhudLmW29mRtT_gcUZELU130_provenance.
- NP681692.RA-vJI5kyJeuxRdzHJ4bIjhnLhudLmW29mRtT_gcUZELU130_assertion wasGeneratedBy ECO_0000203 NP681692.RA-vJI5kyJeuxRdzHJ4bIjhnLhudLmW29mRtT_gcUZELU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP681692.RA-vJI5kyJeuxRdzHJ4bIjhnLhudLmW29mRtT_gcUZELU130_provenance.