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

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Namespace Prefixes

Prefix	IRI
n5	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#
n7	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_2730

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_2731

rdfs:label

epidermolysis bullosa

wdrs:describedby

n5:doid.owl

obo:id

DOID:2730

obo:hasDbXref

SNOMEDCT_US_2021_09_01:205580008 UMLS_CUI:C0014527 GARD:6359 MESH:D004820 ICD10CM:Q81 NCI:C67383

obo:hasExactSynonym

acantholysis bullosa Epidermolysis bullosa

obo:hasOBONamespace

disease_ontology

obo:inSubset

n7:NCIthesaurus

n2:IAO_0000115

A vesiculobullous skin disease that is characterized by formation of blisters with only minor skin trauma, which can cause widespread wounds, dehydration, electrolyte abnormalities, and severe infection, frequently develops_from mutations in connective tissue elements, including genes encoding keratin, collagen, and laminin.