_:vb50940583	<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_0080209>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50940583 .
<http://purl.obolibrary.org/obo/DOID_0080209>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050737> .
<http://purl.obolibrary.org/obo/DOID_0080209>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0080209>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_8955> .
<http://purl.obolibrary.org/obo/DOID_0080209>	<http://www.w3.org/2000/01/rdf-schema#label>	"sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay"@en .
<http://purl.obolibrary.org/obo/DOID_0080209>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:616084"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0080209>	<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_0080209>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0080209"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50940583	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000148> .
<http://purl.obolibrary.org/obo/DOID_0080209>	<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_0080209>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"SIFD"@en .
<http://purl.obolibrary.org/obo/DOID_0080209>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A sideroblastic anemia characterized by onset of severe sideroblastic anemia in the neonatal period or infancy, has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the TRNT1 gene on chromosome 3p26."^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50940583	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .
_:vb50940583	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .