_:vb50936832	<http://www.w3.org/2002/07/owl#annotatedProperty>	<http://purl.obolibrary.org/obo/IAO_0000115> .
_:vb50936832	<http://www.w3.org/2002/07/owl#annotatedSource>	<http://purl.obolibrary.org/obo/DOID_0050434> .
_:vb50936832	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Axiom> .
_:vb50936832	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50936832	<http://purl.org/dc/elements/1.1/type>	<http://purl.obolibrary.org/obo/ECO_0007638> .
_:vb50936832	<http://www.w3.org/2002/07/owl#annotatedTarget>	"A long QT syndrome that has_material_basis_in autosomal dominant inheritance of a mutation in the KCNJ2 gene which disrupts the rhythm of the heart's lower chambers (ventricular arrhythmia) and results_in an unusually small lower jaw (micrognathia), low-set ears, and an abnormal curvature of the fingers called clinodactyly."^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50936832	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:http://en.wikipedia.org/wiki/Long_QT_syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50936832	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:http://en.wikipedia.org/wiki/Andersen%E2%80%93Tawil_syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .