<http://purl.obolibrary.org/obo/DOID_0050477>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A renal tubular transport disease that is characterized by hypertension and hypokalemia caused by dysregulation of epithelial sodium channels causing over expression of the channel."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050477>	<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_0050477>	<http://www.w3.org/2000/01/rdf-schema#comment>	"OMIM mapping confirmed by DO. [SN]."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050477>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0050477"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050477>	<http://www.w3.org/2000/01/rdf-schema#label>	"Liddle syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050477>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:177200"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050477>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_447> .
<http://purl.obolibrary.org/obo/DOID_0050477>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D056929"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050477>	<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_0050477>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C84827"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050477>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:707749005"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050477>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Liddle's syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_0050477>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0221043"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050477>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050477>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:7381"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050477>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Pseudoaldosteronism"@en .
<http://purl.obolibrary.org/obo/DOID_0050477>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#NCIthesaurus> .