This HTML5 document contains 16 embedded RDF statements represented using HTML+Microdata notation.

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

Namespace Prefixes

PrefixIRI
n7https://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_0111036
rdf:type
owl:Class
rdfs:subClassOf
_:vb50944090 n2:DOID_0050736 n2:DOID_13945
rdfs:label
CADASIL 2
wdrs:describedby
n7:doid.owl
obo:id
DOID:0111036
obo:hasDbXref
ICD10CM:F01.1 OMIM:616779
obo:hasExactSynonym
autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 2
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A CADASIL characterized by stroke, transient ischemic attacks, cognitive impairment, dementia, balance impairment, gait disturbance, headaches, and/or seizures associated with early confluent or confluent diffuse white matter hyperintensities that has_material_basis_in heterozygous mutation in the HTRA1 gene on chromosome 10q26.
Subject Item
_:vb50944090
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000147
wdrs:describedby
n7:doid.owl