PropertyValue
?:annID
  • C0338508
?:annLabel
  • Optic Atrophy, Autosomal Dominant
  • Optic atrophy 1
?:annotationFrequency
  • 6 ()
?:annotation_isRelatedTo_Disease
is ?:hasCUIAnnotation of
?:hasGeneratedBy
is ?:relation_isRelatedTo_annotation of
?:sameAs
?:semanticType
  • [dsyn]
?:type

Metadata

Anon_0  
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