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- source_evidence_literature type ECO_0000212 NP973759.RA63FRskE1JlUFnGo3-fFCgemNyP6a1WFoWUExWj5vSn8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP973759.RA63FRskE1JlUFnGo3-fFCgemNyP6a1WFoWUExWj5vSn8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP973759.RA63FRskE1JlUFnGo3-fFCgemNyP6a1WFoWUExWj5vSn8130_provenance.
- NP973759.RA63FRskE1JlUFnGo3-fFCgemNyP6a1WFoWUExWj5vSn8130_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." NP973759.RA63FRskE1JlUFnGo3-fFCgemNyP6a1WFoWUExWj5vSn8130_provenance.
- NP973759.RA63FRskE1JlUFnGo3-fFCgemNyP6a1WFoWUExWj5vSn8130_assertion evidence source_evidence_literature NP973759.RA63FRskE1JlUFnGo3-fFCgemNyP6a1WFoWUExWj5vSn8130_provenance.
- NP973759.RA63FRskE1JlUFnGo3-fFCgemNyP6a1WFoWUExWj5vSn8130_assertion SIO_000772 22491195 NP973759.RA63FRskE1JlUFnGo3-fFCgemNyP6a1WFoWUExWj5vSn8130_provenance.
- NP973759.RA63FRskE1JlUFnGo3-fFCgemNyP6a1WFoWUExWj5vSn8130_assertion wasDerivedFrom befree-2016 NP973759.RA63FRskE1JlUFnGo3-fFCgemNyP6a1WFoWUExWj5vSn8130_provenance.
- NP973759.RA63FRskE1JlUFnGo3-fFCgemNyP6a1WFoWUExWj5vSn8130_assertion wasGeneratedBy ECO_0000203 NP973759.RA63FRskE1JlUFnGo3-fFCgemNyP6a1WFoWUExWj5vSn8130_provenance.
- befree-2016 importedOn "2016-02-19" NP973759.RA63FRskE1JlUFnGo3-fFCgemNyP6a1WFoWUExWj5vSn8130_provenance.