_:vb50947933	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/RO_0002452> .
<http://purl.obolibrary.org/obo/DOID_11723>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#DO_FlyBase_slim> .
_:vb50947931	<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_11723>	<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_11723>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:155095006"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_11723>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:11723"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_11723>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:6291"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_11723>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D020388"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50947933	<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_11723>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50947932	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .
_:vb50947933	<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_11723>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
<http://purl.obolibrary.org/obo/DOID_11723>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50947931 .
<http://purl.obolibrary.org/obo/DOID_11723>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50947932 .
_:vb50947932	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50947931	<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_11723>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50947933 .
_:vb50947931	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_11723>	<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_11723>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_11723>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C75482"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_11723>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:310200"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_11723>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0080012> .
_:vb50947933	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/SYMP_0000363> .
<http://purl.obolibrary.org/obo/DOID_11723>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_9884> .
<http://purl.obolibrary.org/obo/DOID_11723>	<http://www.w3.org/2000/01/rdf-schema#label>	"Duchenne muscular dystrophy"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50947932	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/SYMP_0000094> .
_:vb50947931	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000149> .
<http://purl.obolibrary.org/obo/DOID_11723>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#NCIthesaurus> .
_:vb50947932	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/RO_0002452> .
<http://purl.obolibrary.org/obo/DOID_11723>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Muscular dystrophy, Duchenne"@en .
<http://purl.obolibrary.org/obo/DOID_11723>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0013264"^^<http://www.w3.org/2001/XMLSchema#string> .