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- source_evidence_literature type ECO_0000212 NP973757.RAHyp5z-_fQwar4N23USGEIc0xuh47SsfGCiyVHQU6e-w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP973757.RAHyp5z-_fQwar4N23USGEIc0xuh47SsfGCiyVHQU6e-w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP973757.RAHyp5z-_fQwar4N23USGEIc0xuh47SsfGCiyVHQU6e-w130_provenance.
- NP973757.RAHyp5z-_fQwar4N23USGEIc0xuh47SsfGCiyVHQU6e-w130_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." NP973757.RAHyp5z-_fQwar4N23USGEIc0xuh47SsfGCiyVHQU6e-w130_provenance.
- NP973757.RAHyp5z-_fQwar4N23USGEIc0xuh47SsfGCiyVHQU6e-w130_assertion evidence source_evidence_literature NP973757.RAHyp5z-_fQwar4N23USGEIc0xuh47SsfGCiyVHQU6e-w130_provenance.
- NP973757.RAHyp5z-_fQwar4N23USGEIc0xuh47SsfGCiyVHQU6e-w130_assertion SIO_000772 22491195 NP973757.RAHyp5z-_fQwar4N23USGEIc0xuh47SsfGCiyVHQU6e-w130_provenance.
- NP973757.RAHyp5z-_fQwar4N23USGEIc0xuh47SsfGCiyVHQU6e-w130_assertion wasDerivedFrom befree-2016 NP973757.RAHyp5z-_fQwar4N23USGEIc0xuh47SsfGCiyVHQU6e-w130_provenance.
- NP973757.RAHyp5z-_fQwar4N23USGEIc0xuh47SsfGCiyVHQU6e-w130_assertion wasGeneratedBy ECO_0000203 NP973757.RAHyp5z-_fQwar4N23USGEIc0xuh47SsfGCiyVHQU6e-w130_provenance.
- befree-2016 importedOn "2016-02-19" NP973757.RAHyp5z-_fQwar4N23USGEIc0xuh47SsfGCiyVHQU6e-w130_provenance.