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Namespace Prefixes

Prefix	IRI
n7	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2	http://purl.obolibrary.org/obo/
wdrs	http://www.w3.org/2007/05/powder-s#
rdfs	http://www.w3.org/2000/01/rdf-schema#
obo	http://www.geneontology.org/formats/oboInOwl#
rdf	http://www.w3.org/1999/02/22-rdf-syntax-ns#
owl	http://www.w3.org/2002/07/owl#
xsdh	http://www.w3.org/2001/XMLSchema#

Statements

Subject Item

n2:DOID_0080388

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_0050737 _:vb50940858 n2:DOID_2590

rdfs:label

nephrotic syndrome type 7

wdrs:describedby

n7:doid.owl

obo:id

DOID:0080388

obo:hasDbXref

ORDO:329903 OMIM:615008

obo:hasExactSynonym

Immunoglobulin-mediated MPGN Ig-mediated membranoproliferative glomerulonephritis Ig-mediated MPGN immunoglobulin-mediated membranoproliferative glomerulonephritis nephrotic syndrome type 7 with membranoptoliferative glomerulonephritis

obo:hasOBONamespace

disease_ontology

n2:IAO_0000115

A familial nephrotic syndrome characterized by onset in the first decade of life of progressive renal disease with proteinuria and membranoproliferative glomerulonephritis that has_material_basis_in homozygous or compound heterozygous mutation in the DGKE gene on chromosome 17q22.

Subject Item

_:vb50940858

rdf:type

owl:Restriction

owl:onProperty

n2:IDO_0000664

owl:someValuesFrom

n2:GENO_0000148

wdrs:describedby

n7:doid.owl