<http://purl.obolibrary.org/obo/DOID_0090067>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:2410"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0090067>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0080006> .
_:vb50942197	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .
_:vb50942197	<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_0090067>	<http://www.w3.org/2000/01/rdf-schema#label>	"Fuhrmann syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0090067>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:C538189"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0090067>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050737> .
<http://purl.obolibrary.org/obo/DOID_0090067>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
_:vb50942197	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000148> .
<http://purl.obolibrary.org/obo/DOID_0090067>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:2854"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0090067>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50942197 .
<http://purl.obolibrary.org/obo/DOID_0090067>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:228930"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0090067>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0090067>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0090067"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50942197	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0090067>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A bone development disease that is characterized by bowing of the femora, aplasia or hypoplasia of the fibulae and poly-, oligo-, and syndactyly that has_material_basis_in autosomal recessive inheritance of homozygous mutation in the Wnt family member 7A (WNT7A) gene on chromosome 3p25."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0090067>	<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_0090067>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:Q74.8"^^<http://www.w3.org/2001/XMLSchema#string> .