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

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Namespace Prefixes

Prefix	IRI
n7	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n3	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

n3:DOID_0112038

rdf:type

owl:Class

rdfs:subClassOf

n3:DOID_0080009 _:vb50945962 n3:DOID_0050776

rdfs:label

non-syndromic X-linked intellectual disability 1

wdrs:describedby

n7:doid.owl

obo:id

DOID:0112038

obo:hasDbXref

OMIM:309530 GARD:13221

obo:hasExactSynonym

MRX1 X-linked mental retardation 18 MRX18 X-linked mental retardation 1 X-linked mental retardation 1/78 MRX78 X-linked mental retardation 78

obo:hasOBONamespace

disease_ontology

n3:IAO_0000115

A non-syndromic X-linked intellectual disability characterized by moderate to severe intellectual disability in males and varying levels of intellectual disability in females that has_material_basis_in hemizygous or heterozygous mutation in IQSEC2 on chromosome Xp11.22.

Subject Item

_:vb50945962

rdf:type

owl:Restriction

owl:onProperty

n3:IDO_0000664

owl:someValuesFrom

n3:GENO_0000146

wdrs:describedby

n7:doid.owl