_:vb50938074	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:http://www.ncbi.nlm.nih.gov/gene/204?"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50938074	<http://www.w3.org/2002/07/owl#annotatedSource>	<http://purl.obolibrary.org/obo/DOID_0060020> .
_:vb50938074	<http://purl.org/dc/elements/1.1/type>	<http://purl.obolibrary.org/obo/ECO_0007636> .
_:vb50938074	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Axiom> .
_:vb50938074	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:http://www.ncbi.nlm.nih.gov/gene/11151?ordinalpos=2&itool=EntrezSystem2.PEntrez.Gene.Gene_ResultsPanel.Gene_RVDocSum"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50938074	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50938074	<http://www.w3.org/2002/07/owl#annotatedProperty>	<http://purl.obolibrary.org/obo/IAO_0000115> .
_:vb50938074	<http://www.w3.org/2002/07/owl#annotatedTarget>	"A severe combined immunodeficiency that is the most severe form of SCID and has_material_basis_in mutations in the gene encoding mitochondrial adenylate kinase 2. It is characterized by congenital agranulocytosis, lymphopenia, and lymphoid and thymic hypoplasia with absent cellular and humoral immunity functions."^^<http://www.w3.org/2001/XMLSchema#string> .