This HTML5 document contains 23 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
n8	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#
rdfs	http://www.w3.org/2000/01/rdf-schema#
obo	http://www.geneontology.org/formats/oboInOwl#
n6	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_0050427

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_225 _:vb50936819 n2:DOID_0050737

rdfs:label

xeroderma pigmentosum

rdfs:comment

OMIM mapping confirmed by DO. [SN].

wdrs:describedby

n8:doid.owl

obo:id

DOID:0050427

obo:hasDbXref

NCI:C3452 MESH:D014983 GARD:7910 UMLS_CUI:C0043346 SNOMEDCT_US_2021_09_01:44600005 ICD10CM:Q82.1 ORDO:910

obo:hasOBONamespace

disease_ontology

obo:inSubset

n6:NCIthesaurus n6:DO_FlyBase_slim

n2:IAO_0000115

A syndrome that is characterized by a deficiency in the ability to repair ultraviolet damage that has_material_basis_in autosomal recessive inheritance of DNA repair.

Subject Item

_:vb50936819

rdf:type

owl:Restriction

owl:onProperty

n2:IDO_0000664

owl:someValuesFrom

n2:GENO_0000148

wdrs:describedby

n8:doid.owl