<http://purl.obolibrary.org/obo/DOID_0111946>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50945791	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000147> .
<http://purl.obolibrary.org/obo/DOID_0111946>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50945791 .
_:vb50945791	<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_0111946>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"autosomal dominant chronic mucocutaneous familial candidiasis"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111946>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111946>	<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_0111946>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050736> .
<http://purl.obolibrary.org/obo/DOID_0111946>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50945791	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0111946>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"familial candidiasis 7"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111946>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:614162"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50945791	<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_0111946>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"autosomal dominant immunodeficiency 31C"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111946>	<http://www.w3.org/2000/01/rdf-schema#label>	"immunodeficiency 31C"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111946>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"IMD31C"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111946>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0111946"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111946>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"CANDF7"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111946>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_612> .
<http://purl.obolibrary.org/obo/DOID_0111946>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A primary immunodeficiency disease characterized by onset in infancy or childhood of chronic mucocutaneous candidiasis and increased IFNG activation that has_material_basis_in heterozygous gain of function mutation in STAT1 on chromosome 2q32.2."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111946>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:391487"^^<http://www.w3.org/2001/XMLSchema#string> .