_:vb50951134	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:https://medlineplus.gov/genetics/condition/glycogen-storage-disease-type-v/"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50951134	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Axiom> .
_:vb50951134	<http://www.w3.org/2002/07/owl#annotatedProperty>	<http://purl.obolibrary.org/obo/IAO_0000115> .
_:vb50951134	<http://www.w3.org/2002/07/owl#annotatedTarget>	"A glycogen storage disease that is characterized by onset of exercise intolerance and muscle cramps in childhood or adolescence and that has_material_basis_in homozygous or compound heterozygous mutation in the PYGM gene, which encodes muscle glycogen phosphorylase, on chromosome 11q13."^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50951134	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50951134	<http://www.w3.org/2002/07/owl#annotatedSource>	<http://purl.obolibrary.org/obo/DOID_2746> .