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Prefix	IRI
n5	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n3	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#
n8	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#

Subject Item: n3:DOID_0060452
rdf:type: owl:Class
rdfs:subClassOf: n3:DOID_0050736 _:vb50938866 _:vb50938871 n3:DOID_0060442 n3:DOID_0060388
rdfs:label: posterior amorphous corneal dystrophy
wdrs:describedby: n5:doid.owl
obo:id: DOID:0060452
obo:created_by: elvira
obo:creation_date: 2015-10-16T17:48:04Z
obo:hasDbXref: ORDO:98971 MESH:C567546 ICD10CM:H18.5 OMIM:612868
obo:hasExactSynonym: PACD chromosome 12q21.33 deletion syndrome
obo:hasOBONamespace: disease_ontology
obo:inSubset: n8:DO_rare_slim
n3:IAO_0000115: A stromal dystrophy that is characterized by irregular sheetlike areas of opacification with involvement of the Descemet membrane and, in some instances, alterations of the normal endothelial mosaic and that has_material_basis_in a chromosome 12q21.33 contiguous gene deletion syndrome.