This HTML5 document contains 24 embedded RDF statements represented using HTML+Microdata notation.

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

Namespace Prefixes

PrefixIRI
n4https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2http://purl.obolibrary.org/obo/
wdrshttp://www.w3.org/2007/05/powder-s#
rdfshttp://www.w3.org/2000/01/rdf-schema#
obohttp://www.geneontology.org/formats/oboInOwl#
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
owlhttp://www.w3.org/2002/07/owl#
xsdhhttp://www.w3.org/2001/XMLSchema#

Statements

Subject Item
n2:DOID_0110639
rdf:type
owl:Class
rdfs:subClassOf
_:vb50943352 n2:DOID_0050737 n2:DOID_0050557 _:vb50943351
rdfs:label
congenital muscular dystrophy due to integrin alpha-7 deficiency
wdrs:describedby
n4:doid.owl
obo:id
DOID:0110639
obo:hasDbXref
ORDO:34520 ICD10CM:G71.2 OMIM:613204
obo:hasExactSynonym
congenital myopathy due to integrin alpha-7 deficiency congenital muscular dystrophy with integrin alpha-7 deficiency congenital muscular dystrophy with ITGA7 deficiency
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A congenital muscular dystrophy characterized by autosomal recessive inheritance that has_material_basis_in compound heterozygous mutation in the ITGA7 gene on chromosome 12q13.
Subject Item
_:vb50943351
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000148
wdrs:describedby
n4:doid.owl
Subject Item
_:vb50943352
rdf:type
owl:Restriction
owl:onProperty
n2:RO_0004019
owl:someValuesFrom
n2:HP_0001197
wdrs:describedby
n4:doid.owl