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- source_evidence_literature type ECO_0000212 NP681880.RA5TdN6BwDTuE-hiM95KUbkdIz-ksh-CfuCCLzRGHNi6U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP681880.RA5TdN6BwDTuE-hiM95KUbkdIz-ksh-CfuCCLzRGHNi6U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP681880.RA5TdN6BwDTuE-hiM95KUbkdIz-ksh-CfuCCLzRGHNi6U130_provenance.
- NP681880.RA5TdN6BwDTuE-hiM95KUbkdIz-ksh-CfuCCLzRGHNi6U130_assertion description "[Dominantly transmitted cases had (CAG)(n) expansions at the Machado-Joseph disease gene (MJD1) (63%), at SCA2 (3%), the gene for dentatorubropallidoluysian atrophy (DRPLA) (2%), SCA6 (1%), or SCA7 (1%) loci, or (CTG)(n) expansions at the SCA8 (2%) gene, whereas (GAA)(n) expansions in the Freidreich ataxia gene (FRDA) were found in 64% of families with recessive ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681880.RA5TdN6BwDTuE-hiM95KUbkdIz-ksh-CfuCCLzRGHNi6U130_provenance.
- NP681880.RA5TdN6BwDTuE-hiM95KUbkdIz-ksh-CfuCCLzRGHNi6U130_assertion evidence source_evidence_literature NP681880.RA5TdN6BwDTuE-hiM95KUbkdIz-ksh-CfuCCLzRGHNi6U130_provenance.
- NP681880.RA5TdN6BwDTuE-hiM95KUbkdIz-ksh-CfuCCLzRGHNi6U130_assertion SIO_000772 11939898 NP681880.RA5TdN6BwDTuE-hiM95KUbkdIz-ksh-CfuCCLzRGHNi6U130_provenance.
- NP681880.RA5TdN6BwDTuE-hiM95KUbkdIz-ksh-CfuCCLzRGHNi6U130_assertion wasDerivedFrom befree-20150227 NP681880.RA5TdN6BwDTuE-hiM95KUbkdIz-ksh-CfuCCLzRGHNi6U130_provenance.
- NP681880.RA5TdN6BwDTuE-hiM95KUbkdIz-ksh-CfuCCLzRGHNi6U130_assertion wasGeneratedBy ECO_0000203 NP681880.RA5TdN6BwDTuE-hiM95KUbkdIz-ksh-CfuCCLzRGHNi6U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP681880.RA5TdN6BwDTuE-hiM95KUbkdIz-ksh-CfuCCLzRGHNi6U130_provenance.