This HTML5 document contains 30 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/
n3http://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#
n5http://purl.obolibrary.org/obo/doid#
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
n3:DOID_225
rdf:type
owl:Class
rdfs:subClassOf
n3:DOID_4
owl:equivalentClass
_:vb50950653
rdfs:label
syndrome
wdrs:describedby
n7:doid.owl
obo:id
DOID:225
obo:hasDbXref
MESH:D013577 UMLS_CUI:C0039082 NCI:C28193 SNOMEDCT_US_2021_09_01:64572001
obo:hasOBONamespace
disease_ontology
obo:inSubset
n5:DO_MGI_slim n5:DO_AGR_slim n5:DO_CFDE_slim n5:DO_GXD_slim n5:NCIthesaurus
n3:IAO_0000115
A disease characterized by a group of signs and symptoms that occur together and characterize a particular abnormality.
Subject Item
_:vb50950653
rdf:type
owl:Class
owl:intersectionOf
_:vb50950656
wdrs:describedby
n7:doid.owl
Subject Item
_:vb50950654
rdf:type
owl:Restriction
owl:onProperty
n3:RO_0004019
owl:someValuesFrom
n3:SYMP_0000462
wdrs:describedby
n7:doid.owl
Subject Item
_:vb50950655
rdf:first
_:vb50950654
rdf:rest
rdf:nil
wdrs:describedby
n7:doid.owl
Subject Item
_:vb50950656
rdf:first
n3:DOID_4
rdf:rest
_:vb50950655
wdrs:describedby
n7:doid.owl