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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking MIR7108 and progressive myoclonus epilepsy 9 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127236531|RGD:13466396|RGD:151782547|RGD:152076182|RGD:152092459|RGD:152147327|RGD:152161054|RGD:152175277|RGD:156309945 (Homo sapiens) & RGD:127236531|RGD:13466396|RGD:151782547|RGD:152076182|RGD:152092459|RGD:152147327|RGD:152161054|RGD:152175277|RGD:156309945 (Homo sapiens) & RGD:127236531|RGD:13466396|RGD:151782547|RGD:152076182|RGD:152092459|RGD:152147327|RGD:152161054|RGD:152175277|RGD:156309945 (Homo sapiens) & RGD:127236531|RGD:13466396|RGD:151782547|RGD:152076182|RGD:152092459|RGD:152147327|RGD:152161054|RGD:152175277|RGD:156309945 (Homo sapiens) & RGD:127236531|RGD:13466396|RGD:151782547|RGD:152076182|RGD:152092459|RGD:152147327|RGD:152161054|RGD:152175277|RGD:156309945 (Homo sapiens) & RGD:127236531|RGD:13466396|RGD:151782547|RGD:152076182|RGD:152092459|RGD:152147327|RGD:152161054|RGD:152175277|RGD:156309945 (Homo sapiens) & RGD:127236531|RGD:13466396|RGD:151782547|RGD:152076182|RGD:152092459|RGD:152147327|RGD:152161054|RGD:152175277|RGD:156309945 (Homo sapiens) & RGD:127236531|RGD:13466396|RGD:151782547|RGD:152076182|RGD:152092459|RGD:152147327|RGD:152161054|RGD:152175277|RGD:156309945 (Homo sapiens) & RGD:127236531|RGD:13466396|RGD:151782547|RGD:152076182|RGD:152092459|RGD:152147327|RGD:152161054|RGD:152175277|RGD:156309945 (Homo sapiens)
  • 40 RGD objects have been annotated to progressive myoclonus epilepsy 9  (DOID:0111450)
  • 0 papers in RGD have been used to annotate MIR7108
  • Curation Notes: ClinVar Annotator: match by term: Progressive myoclonic epilepsy type 9
  • Original References(s): PMID:28492532


    • An association has been curated linking MIR7108 and progressive myoclonus epilepsy 9 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13625023 (Homo sapiens)
  • 40 RGD objects have been annotated to progressive myoclonus epilepsy 9  (DOID:0111450)
  • 0 papers in RGD have been used to annotate MIR7108
  • Curation Notes: ClinVar Annotator: match by term: Progressive myoclonic epilepsy type 9
  • Original References(s): PMID:25741868 PMID:28492532


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