_:vb50936905	<http://purl.org/dc/elements/1.1/type>	<http://purl.obolibrary.org/obo/ECO_0007638> .
_:vb50936905	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:http://en.wikipedia.org/wiki/Barth_syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50936905	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:http://www.rarediseases.org/rare-disease-information/rare-diseases/byID/1116/viewAbstract"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50936905	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50936905	<http://www.w3.org/2002/07/owl#annotatedSource>	<http://purl.obolibrary.org/obo/DOID_0050476> .
_:vb50936905	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:http://rarediseases.info.nih.gov/gard/5890/barth-syndrome/resources/1"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50936905	<http://www.w3.org/2002/07/owl#annotatedProperty>	<http://purl.obolibrary.org/obo/IAO_0000115> .
_:vb50936905	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Axiom> .
_:vb50936905	<http://purl.org/dc/elements/1.1/type>	<http://purl.obolibrary.org/obo/ECO_0007636> .
_:vb50936905	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:http://www.ninds.nih.gov/disorders/barth/barth.htm"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50936905	<http://www.w3.org/2002/07/owl#annotatedTarget>	"A lipid metabolism disorder that has_material_basis_in X-linked inheritance of the tafazzin gene and is characterized by decreased production of an enzyme required to produce cardiolipin."^^<http://www.w3.org/2001/XMLSchema#string> .