_:vb50945543	<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_0111822>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:17608003"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111822>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111822>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0080009> .
<http://purl.obolibrary.org/obo/DOID_0111822>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0265267"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111822>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:6039"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50945543	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000146> .
<http://purl.obolibrary.org/obo/DOID_0111822>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_225> .
<http://purl.obolibrary.org/obo/DOID_0111822>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50945543 .
<http://purl.obolibrary.org/obo/DOID_0111822>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:139"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111822>	<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_0111822>	<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_0111822>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"CHILD nevus"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111822>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A syndrome characterized by congenital hemidysplasia, ichythyosiform erythrodema, and limb defects that has_material_basis_in heterozygous mutation in NSDHL on chromosome Xq28."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111822>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:C562515"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111822>	<http://www.w3.org/2000/01/rdf-schema#label>	"CHILD syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111822>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:308050"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111822>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"congenital hemidysplasia with ichthyosiform nevus and limbs defects"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50945543	<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_0111822>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0111822"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50945543	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .