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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_0007636
annotatedProperty	http://purl.obolibrary.org/obo/IAO_0000115
annotatedSource	pontocerebellar hypoplasia type 8
annotatedTarget	A pontocerebellar hypoplasia that is characterized by delayed psychomotor development, chorea, hypotonia, spasticity and visual defects, has_material_basis_in autosomal recessive inheritance of mutation in the CHMP1A gene.
database_cross_reference	url:https://www.omim.org/entry/614961
is topic of	Human Disease Ontology

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