<http://purl.obolibrary.org/obo/DOID_0111937>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50945773	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000148> .
<http://purl.obolibrary.org/obo/DOID_0111937>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_627> .
<http://purl.obolibrary.org/obo/DOID_0111937>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"severe combined immunodeficiency due to lymphocyte-specific protein tyrosine kinase deficiency"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111937>	<http://www.w3.org/2000/01/rdf-schema#label>	"immunodeficiency 22"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111937>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C4014233"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50945773	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0111937>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050737> .
<http://purl.obolibrary.org/obo/DOID_0111937>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"IMD22"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50945773	<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_0111937>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0111937"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50945773	<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_0111937>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50945773 .
<http://purl.obolibrary.org/obo/DOID_0111937>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A severe combined immunodeficiency characterized by severe combined immunodeficiency, selective CD4 lymphopenia, and lack of CD28 expression on CD8+ T cells that has_material_basis_in homozygous or compound heterozygous mutation in LCK on chromosome 1p35.2."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111937>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111937>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:615758"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111937>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"SCID due to lymphocyte-specific protein tyrosine kinase deficiency"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111937>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"severe combined immunodeficiency due to LCK deficiency"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111937>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C176808"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111937>	<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_0111937>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:280142"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111937>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"SCID due to LCK deficiency"^^<http://www.w3.org/2001/XMLSchema#string> .