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- source_evidence_literature type ECO_0000212 NP342937.RAGQo69Nu7KT8OfFrpJO8xz15uSiyRHC7YmLtdTyh77Hs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP342937.RAGQo69Nu7KT8OfFrpJO8xz15uSiyRHC7YmLtdTyh77Hs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP342937.RAGQo69Nu7KT8OfFrpJO8xz15uSiyRHC7YmLtdTyh77Hs130_provenance.
- befree-2016 importedOn "2016-02-19" NP342937.RAGQo69Nu7KT8OfFrpJO8xz15uSiyRHC7YmLtdTyh77Hs130_provenance.
- NP342937.RAGQo69Nu7KT8OfFrpJO8xz15uSiyRHC7YmLtdTyh77Hs130_assertion wasGeneratedBy ECO_0000203 NP342937.RAGQo69Nu7KT8OfFrpJO8xz15uSiyRHC7YmLtdTyh77Hs130_provenance.
- NP342937.RAGQo69Nu7KT8OfFrpJO8xz15uSiyRHC7YmLtdTyh77Hs130_assertion wasDerivedFrom befree-2016 NP342937.RAGQo69Nu7KT8OfFrpJO8xz15uSiyRHC7YmLtdTyh77Hs130_provenance.
- NP342937.RAGQo69Nu7KT8OfFrpJO8xz15uSiyRHC7YmLtdTyh77Hs130_assertion SIO_000772 11807410 NP342937.RAGQo69Nu7KT8OfFrpJO8xz15uSiyRHC7YmLtdTyh77Hs130_provenance.
- NP342937.RAGQo69Nu7KT8OfFrpJO8xz15uSiyRHC7YmLtdTyh77Hs130_assertion evidence source_evidence_literature NP342937.RAGQo69Nu7KT8OfFrpJO8xz15uSiyRHC7YmLtdTyh77Hs130_provenance.
- NP342937.RAGQo69Nu7KT8OfFrpJO8xz15uSiyRHC7YmLtdTyh77Hs130_assertion description "[We have analyzed six trinucleotide repeat-containing loci [spinocerebellar ataxias (SCA1, SCA3, SCA8), dentatorubral-pallidoluysian atrophy (DRPLA), Huntington chorea (HD) and fragile X syndrome (FRAXA)] in myotonic dystrophy type 1 (DM1) patients (n = 52).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP342937.RAGQo69Nu7KT8OfFrpJO8xz15uSiyRHC7YmLtdTyh77Hs130_provenance.