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- source_evidence_literature type ECO_0000212 NP929523.RAuX1Mm-OHmQdUsWsl-StSMEXfi7rgt9L_dBSrrbhXNRA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP929523.RAuX1Mm-OHmQdUsWsl-StSMEXfi7rgt9L_dBSrrbhXNRA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP929523.RAuX1Mm-OHmQdUsWsl-StSMEXfi7rgt9L_dBSrrbhXNRA130_provenance.
- NP929523.RAuX1Mm-OHmQdUsWsl-StSMEXfi7rgt9L_dBSrrbhXNRA130_assertion description "[The growing list ofneurodegenerative and neuromuscular diseases caused by dynamic mutations includes Huntington's disease (HD), spinobulbar muscular atrophy (SBMA), dentatorubral-pallidoluysian atrophy (DRPLA), a number of spinocerebellar ataxias (SCAs), oculopharyngeal muscular dystrophy (OPMD), myotonic dystrophy Type 1 and 2 (DM1 and 2), Huntington's disease-like 2 (HDL-2), Friedrich's ataxia (FRDA), Fragile X associated tremor ataxia syndrome (FXTAS), Fragile XE (FRAXE) and Fragile XA (FRAXA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP929523.RAuX1Mm-OHmQdUsWsl-StSMEXfi7rgt9L_dBSrrbhXNRA130_provenance.
- NP929523.RAuX1Mm-OHmQdUsWsl-StSMEXfi7rgt9L_dBSrrbhXNRA130_assertion evidence source_evidence_literature NP929523.RAuX1Mm-OHmQdUsWsl-StSMEXfi7rgt9L_dBSrrbhXNRA130_provenance.
- NP929523.RAuX1Mm-OHmQdUsWsl-StSMEXfi7rgt9L_dBSrrbhXNRA130_assertion SIO_000772 23560305 NP929523.RAuX1Mm-OHmQdUsWsl-StSMEXfi7rgt9L_dBSrrbhXNRA130_provenance.
- NP929523.RAuX1Mm-OHmQdUsWsl-StSMEXfi7rgt9L_dBSrrbhXNRA130_assertion wasDerivedFrom befree-20150227 NP929523.RAuX1Mm-OHmQdUsWsl-StSMEXfi7rgt9L_dBSrrbhXNRA130_provenance.
- NP929523.RAuX1Mm-OHmQdUsWsl-StSMEXfi7rgt9L_dBSrrbhXNRA130_assertion wasGeneratedBy ECO_0000203 NP929523.RAuX1Mm-OHmQdUsWsl-StSMEXfi7rgt9L_dBSrrbhXNRA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP929523.RAuX1Mm-OHmQdUsWsl-StSMEXfi7rgt9L_dBSrrbhXNRA130_provenance.