<http://purl.obolibrary.org/obo/DOID_630>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_4> .
<http://purl.obolibrary.org/obo/DOID_630>	<http://www.w3.org/2002/07/owl#equivalentClass>	_:vb50954693 .
<http://purl.obolibrary.org/obo/DOID_630>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A disease that has_material_basis_in genetic variations in the human genome."^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50954694	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50954694	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/SO_0001537> .
<http://purl.obolibrary.org/obo/DOID_630>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D030342"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50954695	<http://www.w3.org/1999/02/22-rdf-syntax-ns#first>	_:vb50954694 .
_:vb50954696	<http://www.w3.org/1999/02/22-rdf-syntax-ns#first>	<http://purl.obolibrary.org/obo/DOID_4> .
<http://purl.obolibrary.org/obo/DOID_630>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50954696	<http://www.w3.org/1999/02/22-rdf-syntax-ns#rest>	_:vb50954695 .
<http://purl.obolibrary.org/obo/DOID_630>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#NCIthesaurus> .
_:vb50954694	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .
_:vb50954696	<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_630>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#DO_RAD_slim> .
_:vb50954693	<http://www.w3.org/2002/07/owl#intersectionOf>	_:vb50954696 .
<http://purl.obolibrary.org/obo/DOID_630>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:630"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_630>	<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_630>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#DO_CFDE_slim> .
<http://purl.obolibrary.org/obo/DOID_630>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0019247"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_630>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C3101"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50954693	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
_:vb50954693	<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_630>	<http://www.w3.org/2000/01/rdf-schema#label>	"genetic disease"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_630>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50954695	<http://www.w3.org/1999/02/22-rdf-syntax-ns#rest>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#nil> .
_:vb50954694	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/RO_0004019> .
_:vb50954695	<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_630>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:32895009"^^<http://www.w3.org/2001/XMLSchema#string> .