_:vb50938007	<http://www.w3.org/2002/07/owl#annotatedTarget>	"An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, intellectual disability, dysarthria and ophthalmoplegia, and has_material_basis_in mutation in the ITPR1 gene."^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50938007	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Axiom> .
_:vb50938007	<http://purl.org/dc/elements/1.1/type>	<http://purl.obolibrary.org/obo/ECO_0007637> .
_:vb50938007	<http://www.w3.org/2002/07/owl#annotatedProperty>	<http://purl.obolibrary.org/obo/IAO_0000115> .
_:vb50938007	<http://www.w3.org/2002/07/owl#annotatedSource>	<http://purl.obolibrary.org/obo/DOID_0050978> .
_:vb50938007	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:https://rarediseases.info.nih.gov/diseases/10480/spinocerebellar-ataxia-29"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50938007	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .