<http://purl.obolibrary.org/obo/DOID_0080390>	<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_0080390>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0080390"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50940862	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .
_:vb50940862	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0080390>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:256300"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50940862	<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_0080390>	<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_0080390>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:1500"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0080390>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:839"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0080390>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Finnish congenital nephrosis"@en .
<http://purl.obolibrary.org/obo/DOID_0080390>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050737> .
<http://purl.obolibrary.org/obo/DOID_0080390>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C122795"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0080390>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MEDDRA:10060740"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0080390>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A familial nephrotic syndrome characterized by prenatal onset of massive proteinuria followed by steroid resistant renal disease that has_material_basis_in homozygous or compound heterozygous mutation in the NPHS1 gene on chromosome 19q13."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0080390>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0080390>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_2590> .
<http://purl.obolibrary.org/obo/DOID_0080390>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50940862 .
_:vb50940862	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000148> .
<http://purl.obolibrary.org/obo/DOID_0080390>	<http://www.w3.org/2000/01/rdf-schema#label>	"nephrotic syndrome type 1"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0080390>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:197601003"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0080390>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0403399"^^<http://www.w3.org/2001/XMLSchema#string> .