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- source_evidence_literature type ECO_0000212 NP584267.RAmZHuCMbOBHcrTHeq3KpuggLNDtitEhrSfkjrdk2Hy8U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584267.RAmZHuCMbOBHcrTHeq3KpuggLNDtitEhrSfkjrdk2Hy8U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584267.RAmZHuCMbOBHcrTHeq3KpuggLNDtitEhrSfkjrdk2Hy8U130_provenance.
- NP584267.RAmZHuCMbOBHcrTHeq3KpuggLNDtitEhrSfkjrdk2Hy8U130_assertion description "[However, mutations inATP13A2, PLA2G6 and FBX07 are often associated with rapidly progressive parkinsonism and with additional features including pyramidal signs, cognitive decline and loss of sustained Levodopa responsiveness.Clarifying the phenotypes of each of these autosomal-recessive parkinsonian-pyramidal syndromes and understanding the mechanism ot these causative gene products might illuminate the pathogenesis of dopaminergic neuronal degeneration also in the common forms of PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584267.RAmZHuCMbOBHcrTHeq3KpuggLNDtitEhrSfkjrdk2Hy8U130_provenance.
- NP584267.RAmZHuCMbOBHcrTHeq3KpuggLNDtitEhrSfkjrdk2Hy8U130_assertion evidence source_evidence_literature NP584267.RAmZHuCMbOBHcrTHeq3KpuggLNDtitEhrSfkjrdk2Hy8U130_provenance.
- NP584267.RAmZHuCMbOBHcrTHeq3KpuggLNDtitEhrSfkjrdk2Hy8U130_assertion SIO_000772 23196729 NP584267.RAmZHuCMbOBHcrTHeq3KpuggLNDtitEhrSfkjrdk2Hy8U130_provenance.
- NP584267.RAmZHuCMbOBHcrTHeq3KpuggLNDtitEhrSfkjrdk2Hy8U130_assertion wasDerivedFrom befree-20140225 NP584267.RAmZHuCMbOBHcrTHeq3KpuggLNDtitEhrSfkjrdk2Hy8U130_provenance.
- NP584267.RAmZHuCMbOBHcrTHeq3KpuggLNDtitEhrSfkjrdk2Hy8U130_assertion wasGeneratedBy ECO_0000203 NP584267.RAmZHuCMbOBHcrTHeq3KpuggLNDtitEhrSfkjrdk2Hy8U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP584267.RAmZHuCMbOBHcrTHeq3KpuggLNDtitEhrSfkjrdk2Hy8U130_provenance.