<http://purl.obolibrary.org/obo/DOID_0060885>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0060885"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060885>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:34528"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060885>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"HOMG2"@en .
<http://purl.obolibrary.org/obo/DOID_0060885>	<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_0060885>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060885>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"autosomal dominant primary hypomagnesemia with hypocalciuria"@en .
<http://purl.obolibrary.org/obo/DOID_0060885>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0060879> .
<http://purl.obolibrary.org/obo/DOID_0060885>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:154020"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060885>	<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_0060885>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:3350"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060885>	<http://www.w3.org/2000/01/rdf-schema#label>	"renal hypomagnesemia 2"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060885>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:E83.4"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060885>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A hypomagnesemia characterized by autosomal dominant inheritance of hypomagnesemia due to renal magnesium loss that has material_basis_in heterozygous mutation in the FXYD2 gene on chromosome 11q23."^^<http://www.w3.org/2001/XMLSchema#string> .