This HTML5 document contains 22 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

Prefix	IRI
n8	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#
n6	http://purl.obolibrary.org/obo/doid#
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_0060364

rdf:type

owl:Class

rdfs:subClassOf

_:vb50938720 n2:DOID_0050737 n2:DOID_0080694

rdfs:label

Galloway-Mowat syndrome 1

wdrs:describedby

n8:doid.owl

obo:id

DOID:0060364

obo:created_by

elvira

obo:creation_date

2015-09-17T16:00:31Z

obo:hasDbXref

OMIM:251300

obo:hasExactSynonym

Galloway syndrome nephrosis-microcephaly syndrome nephrosis-neuronal dysmigration syndrome microcephaly, hiatal hernia and nephrotic syndrome

obo:hasOBONamespace

disease_ontology

obo:inSubset

n6:DO_rare_slim n6:NCIthesaurus

n2:IAO_0000115

A Galloway-Mowat syndrome that has_material_basis_in homozygous mutation in the WDR73 gene on chromosome 15q25.

Subject Item

_:vb50938720

rdf:type

owl:Restriction

owl:onProperty

n2:IDO_0000664

owl:someValuesFrom

n2:GENO_0000148

wdrs:describedby

n8:doid.owl