PropertyValue
?:annID
  • C0000772
?:annLabel
  • Multiple congenital anomalies
?:annotationFrequency
  • 9 ()
?:annotation_isRelatedTo_Disease
is ?:hasCUIAnnotation of
?:hasGeneratedBy
is ?:hasInteractingPhenotype of
is ?:relation_isRelatedTo_annotation of
?:sameAs
?:semanticType
  • [cgab]
?:type

Metadata

Anon_0  
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