_:vb50937118	<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_0050560>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050737> .
<http://purl.obolibrary.org/obo/DOID_0050560>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0050560"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050560>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050557> .
_:vb50937118	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0050560>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050560>	<http://www.w3.org/2000/01/rdf-schema#label>	"Walker-Warburg syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050560>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:2599"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050560>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A congenital muscular dystrophy that is characterized by hypotonia, seizures, severe intellectual and developmental disability, eye abnormalities and early death and has_material_basis_in mutations in multiple genes including POMT1, POMT2, ISPD, FKTN, FKRP, and LARGE1."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050560>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#DO_FlyBase_slim> .
_:vb50937118	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000148> .
<http://purl.obolibrary.org/obo/DOID_0050560>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50937118 .
<http://purl.obolibrary.org/obo/DOID_0050560>	<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_0050560>	<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_0050560>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D058494"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050560>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"cerebroocular dysplasia-muscular dystrophy syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_0050560>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"HARD syndrome"@en .
_:vb50937118	<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_0050560>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .