<http://purl.obolibrary.org/obo/DOID_2748>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050737> .
_:vb50951136	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
<http://purl.obolibrary.org/obo/DOID_2748>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:232400"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50951136	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000148> .
<http://purl.obolibrary.org/obo/DOID_2748>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50951136 .
<http://purl.obolibrary.org/obo/DOID_2748>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#NCIthesaurus> .
<http://purl.obolibrary.org/obo/DOID_2748>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
_:vb50951136	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_2748>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C84736"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2748>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
<http://purl.obolibrary.org/obo/DOID_2748>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_2747> .
<http://purl.obolibrary.org/obo/DOID_2748>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:2748"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2748>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Glycogen storage disease, type III"@en .
<http://purl.obolibrary.org/obo/DOID_2748>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2748>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:E74.03"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2748>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D006010"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2748>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0017922"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2748>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:66937008"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2748>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"amylo 1,6 glucosidase deficiency"@en .
_:vb50951136	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .
<http://purl.obolibrary.org/obo/DOID_2748>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"deficiency of debranching enzyme"@en .
<http://purl.obolibrary.org/obo/DOID_2748>	<http://www.w3.org/2000/01/rdf-schema#comment>	"OMIM mapping confirmed by DO. [SN]."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2748>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A glycogen storage disease that is characterized by an accumulation of abnormal glycogen with short outer chains and that has_material_basis_in homozygous or compound heterozygous mutation in the AGL gene, which encodes the glycogen debrancher enzyme, on chromosome 1p21."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2748>	<http://www.w3.org/2000/01/rdf-schema#label>	"glycogen storage disease III"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2748>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"deficiency of dextrin"@en .