<http://purl.obolibrary.org/obo/DOID_11725>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:199"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_11725>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C75016"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_11725>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_11725>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"De Lange syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_11725>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:40354009"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_11725>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050177> .
_:vb50947936	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/SO_0000704> .
<http://purl.obolibrary.org/obo/DOID_11725>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:PS122470"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_11725>	<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_11725>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Brachmann de Lange syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_11725>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A syndrome that is characterized by slow growth before and after birth, intellectual disability that is usually severe to profound, skeletal abnormalities involving the arms and hands, and distinctive facial features."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_11725>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_225> .
<http://purl.obolibrary.org/obo/DOID_11725>	<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_11725>	<http://www.w3.org/2000/01/rdf-schema#comment>	"Xref MGI.\nOMIM mapping confirmed by DO. [SN]."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_11725>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50947936 .
_:vb50947936	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/RO_0004019> .
<http://purl.obolibrary.org/obo/DOID_11725>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:10109"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_11725>	<http://www.w3.org/2000/01/rdf-schema#label>	"Cornelia de Lange syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50947936	<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_11725>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#DO_rare_slim> .
<http://purl.obolibrary.org/obo/DOID_11725>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0270972"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_11725>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D003635"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_11725>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:Q87.19"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_11725>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#NCIthesaurus> .
_:vb50947936	<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_11725>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:11725"^^<http://www.w3.org/2001/XMLSchema#string> .