<http://purl.obolibrary.org/obo/DOID_0110142>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"BARTS1"@en .
<http://purl.obolibrary.org/obo/DOID_0110142>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110142>	<http://www.w3.org/2000/01/rdf-schema#label>	"Bartter disease type 1"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110142>	<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_0110142>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Bartter syndrome type 1 antenatal"@en .
<http://purl.obolibrary.org/obo/DOID_0110142>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"hypokalemic alkalosis with hypercalciuria 1 antenatal"@en .
<http://purl.obolibrary.org/obo/DOID_0110142>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0110142"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110142>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the sodium-potassium-chloride cotransporter-2 gene (SLC12A1) on chromosome 15q21."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110142>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"hyperprostaglandin E syndrome 1"@en .
<http://purl.obolibrary.org/obo/DOID_0110142>	<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_0110142>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_445> .
<http://purl.obolibrary.org/obo/DOID_0110142>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:601678"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110142>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Bartter syndrome type 1"@en .
<http://purl.obolibrary.org/obo/DOID_0110142>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:E26.8"^^<http://www.w3.org/2001/XMLSchema#string> .