<http://purl.obolibrary.org/obo/DOID_0111970>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A T cell and NK cell immunodeficiency characterized by onset in childhood of recurrent infections due to defective T- and NK-cell function that has_material_basis_in homozygous or compound heterozygous mutation in STIM1 on chromosome 11p15.4."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111970>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0111970"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50945834	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000148> .
<http://purl.obolibrary.org/obo/DOID_0111970>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0080710> .
<http://purl.obolibrary.org/obo/DOID_0111970>	<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_0111970>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"CID due to STIM1 deficiency"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111970>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:612783"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111970>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C2748557"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50945834	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0111970>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50945834 .
<http://purl.obolibrary.org/obo/DOID_0111970>	<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_0111970>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"immune dysfunction with T-cell inactivation due to calcium entry defect 2"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111970>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050737> .
_:vb50945834	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50945834	<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_0111970>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"IMD10"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111970>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:C557827"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111970>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"STIM1 deficiency"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111970>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:317430"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111970>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111970>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"combined immunodeficiency due to STIM1 deficiency"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111970>	<http://www.w3.org/2000/01/rdf-schema#label>	"immunodeficiency 10"^^<http://www.w3.org/2001/XMLSchema#string> .