_:vb50942123	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Axiom> .
_:vb50942123	<http://www.w3.org/2002/07/owl#annotatedSource>	<http://purl.obolibrary.org/obo/DOID_0090031> .
_:vb50942123	<http://purl.org/dc/elements/1.1/type>	<http://purl.obolibrary.org/obo/ECO_0007637> .
_:vb50942123	<http://purl.org/dc/elements/1.1/type>	<http://purl.obolibrary.org/obo/ECO_0007636> .
_:vb50942123	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:https://www.omim.org/entry/261515"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50942123	<http://www.w3.org/2002/07/owl#annotatedTarget>	"A peroxisomal disease characterized by, in severe cases, infantile-onset of hypotonia, seizures, and abnormal facial features with most dieing before age 2 years that has_material_basis_in homozygous or compound heterozygous mutation in the HSD17B4 gene on chromosome 5q2."^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50942123	<http://www.w3.org/2002/07/owl#annotatedProperty>	<http://purl.obolibrary.org/obo/IAO_0000115> .
_:vb50942123	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:https://ghr.nlm.nih.gov/condition/d-bifunctional-protein-deficiency"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50942123	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .