This HTML5 document contains 29 embedded RDF statements represented using HTML+Microdata notation.

The embedded RDF content will be recognized by any processor of HTML5 Microdata.

Namespace Prefixes

Prefix	IRI
n9	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#
skos	http://www.w3.org/2004/02/skos/core#
rdfs	http://www.w3.org/2000/01/rdf-schema#
obo	http://www.geneontology.org/formats/oboInOwl#
n7	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_0050476

rdf:type

owl:Class

rdfs:subClassOf

_:vb50936904 n2:DOID_0080012 n2:DOID_3146

rdfs:label

Barth syndrome

rdfs:comment

OMIM mapping confirmed by DO. [SN].

skos:exactMatch

MESH:D056889

wdrs:describedby

n9:doid.owl

obo:id

DOID:0050476

obo:hasDbXref

NCI:C84585 OMIM:302060 MESH:D056889 GARD:5890 ICD10CM:E78.71 SNOMEDCT_US_2021_09_01:297231002 UMLS_CUI:C0574083

obo:hasExactSynonym

MGA type II 3-methylglutaconicaciduria type 2 3-methylglutaconicaciduria type II MGA Type 2

obo:hasOBONamespace

disease_ontology

obo:inSubset

n7:DO_FlyBase_slim n7:DO_rare_slim n7:NCIthesaurus

n2:IAO_0000115

A lipid metabolism disorder that has_material_basis_in X-linked inheritance of the tafazzin gene and is characterized by decreased production of an enzyme required to produce cardiolipin.

Subject Item

_:vb50936904

rdf:type

owl:Restriction

owl:onProperty

n2:IDO_0000664

owl:someValuesFrom

n2:GENO_0000149

wdrs:describedby

n9:doid.owl