About: paroxysmal nonkinesigenic dyskinesia 1

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

Attributes	Values
type	Class
subClassOf	autosomal dominant disease dystonia nodeID://b50942161 nodeID://b50942162
label	paroxysmal nonkinesigenic dyskinesia 1
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0090049
database_cross_reference	ICD10CM:G24.8 OMIM:118800 ORDO:98810
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A dystonia that is characterized by attacks of dystonic or choreathetotic movements precipitated by stress, fatigue, coffee or alcohol intake or menstruation, and has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the PNKD metallo-beta-lactamase domain containing gene on chromosome 2q35.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50942163

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