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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_0007637
annotatedProperty	http://purl.obolibrary.org/obo/IAO_0000115
annotatedSource	aspartylglucosaminuria
annotatedTarget	A lysosomal storage disease that is characterized by delayed speech at 2-3 years of age, has_material_basis_in mutations in the AGA gene that result in the absence or shortage of the aspartylglucosaminidase enzyme in lysosomes, preventing the normal breakdown of glycoproteins.
database_cross_reference	url:https://ghr.nlm.nih.gov/condition/aspartylglucosaminuria
is topic of	Human Disease Ontology

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