_:vb50945799	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0111950>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050737> .
_:vb50945799	<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_0111950>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"MSMD due to complete IL12B deficiency"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111950>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:614890"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111950>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111950>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0111950"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111950>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"IMD29"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111950>	<http://www.w3.org/2000/01/rdf-schema#label>	"immunodeficiency 29"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50945799	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000148> .
<http://purl.obolibrary.org/obo/DOID_0111950>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_612> .
<http://purl.obolibrary.org/obo/DOID_0111950>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Mendelian susceptibility to mycobacterial diseases due to complete interleukin 12B deficiency"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111950>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50945799 .
<http://purl.obolibrary.org/obo/DOID_0111950>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111950>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:319558"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111950>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"IL12B deficiency"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111950>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"immunodeficiency 29, mycobacteriosis"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50945799	<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_0111950>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"MSMD due to complete interleukin 12B deficiency"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111950>	<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_0111950>	<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_0111950>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A primary immunodeficiency disease characterized by undetectable IL12B secretion by leukocytes and increased susceptibility to intracellular bacterial infections that has_material_basis_in homozygous or compound heterozygous mutation in IL12B on chromosome 5q33.3."^^<http://www.w3.org/2001/XMLSchema#string> .