<http://purl.obolibrary.org/obo/DOID_13087>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD9CM:426.81"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13087>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"atrial tachyarrhythmia with short PR interval"@en .
<http://purl.obolibrary.org/obo/DOID_13087>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:I45.6"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13087>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:108950"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13087>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_225> .
<http://purl.obolibrary.org/obo/DOID_13087>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"syndrome of short P-R interval, normal QRS complexes, and supraventricular tachycardias"@en .
<http://purl.obolibrary.org/obo/DOID_13087>	<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_13087>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0024054"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13087>	<http://www.w3.org/2000/01/rdf-schema#label>	"Lown-Ganong-Levine syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13087>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A syndrome that involves pre-excitation of the ventricles due to an accessory pathway providing an abnormal electrical communication from the atria to the ventricles."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13087>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:844"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13087>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D008151"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13087>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#DO_rare_slim> .
<http://purl.obolibrary.org/obo/DOID_13087>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13087>	<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_13087>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:13087"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13087>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:55475008"^^<http://www.w3.org/2001/XMLSchema#string> .