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

Attributes	Values
type	Axiom
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
Type	http://purl.obolibrary.org/obo/ECO_0007645
annotatedProperty	http://purl.obolibrary.org/obo/IAO_0000115
annotatedSource	developmental and epileptic encephalopathy 9
annotatedTarget	A developmental and epileptic encephalopathy characterized by seizure onset in infancy and mild to severe intellectual impairment in females that has_material_basis_in heterozygous mutation in the gene encoding protocadherin-19 (PCDH19) on chromosome Xq22.
database_cross_reference	url:https://pubmed.ncbi.nlm.nih.gov/20830798/ url:https://www.ncbi.nlm.nih.gov/pubmed/18469813 url:https://www.ncbi.nlm.nih.gov/pubmed/19752159
is topic of	Human Disease Ontology

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