This HTML5 document contains 35 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

PrefixIRI
n6https://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_0111860
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_225 _:vb50945616 n2:DOID_0060388
rdfs:label
AMME complex
wdrs:describedby
n6:doid.owl
obo:id
DOID:0111860
obo:hasDbXref
ORDO:86818 SNOMEDCT_US_2021_09_01:720982007 OMIM:300194 MESH:C564570 UMLS_CUI:C1846242
obo:hasExactSynonym
Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome chromosome Xq22.3 telomeric deletion syndrome AMME syndrome ATS-MR
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A syndrome characterized by Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis that has_material_basis_in hemizygous deletion of multiple genes including COL4A5, FACL4 and AMMECR1 on chromosome Xq22.3.
Subject Item
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owl:intersectionOf
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owl:someValuesFrom
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Subject Item
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Subject Item
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