<http://purl.obolibrary.org/obo/DOID_0110221>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:I49.8"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110221>	<http://www.w3.org/2000/01/rdf-schema#label>	"Brugada syndrome 4"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110221>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:611876"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110221>	<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_0110221>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:10362"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110221>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A Brugada syndrome that has_material_basis_in heterozygous mutation in the gene encoding the beta-2 subunit of the voltage-dependent L-type calcium channel (CACNB2) on chromosome 10p12."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110221>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050451> .
<http://purl.obolibrary.org/obo/DOID_0110221>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110221>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"BRGDA4"@en .
<http://purl.obolibrary.org/obo/DOID_0110221>	<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_0110221>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0110221"^^<http://www.w3.org/2001/XMLSchema#string> .