This HTML5 document contains 25 embedded RDF statements represented using HTML+Microdata notation.

The embedded RDF content will be recognized by any processor of HTML5 Microdata.

Namespace Prefixes

PrefixIRI
n5https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n3http://purl.obolibrary.org/obo/
wdrshttp://www.w3.org/2007/05/powder-s#
skoshttp://www.w3.org/2004/02/skos/core#
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
n3:DOID_0050462
rdf:type
owl:Class
rdfs:subClassOf
n3:DOID_2340 _:vb50936872 n3:DOID_225 n3:DOID_0050737 _:vb50936871
rdfs:label
Antley-Bixler syndrome
rdfs:comment
OMIM mapping confirmed by DO. [SN].
skos:exactMatch
MESH:D054882
wdrs:describedby
n5:doid.owl
obo:id
DOID:0050462
obo:hasDbXref
OMIM:201750 OMIM:207410 SNOMEDCT_US_2020_03_01:62964007
obo:hasExactSynonym
trapezoidocephaly-synostosis syndrome
obo:hasOBONamespace
disease_ontology
n3:IAO_0000115
A craniosynostosis that is characterized at birth or prenatally by malformations and deformities affecting the majority of the skeleton and other areas of the body with autosomal recessive inheritance of the FGFR2 gene.
Subject Item
_:vb50936871
rdf:type
owl:Restriction
owl:onProperty
n3:IDO_0000664
owl:someValuesFrom
n3:GENO_0000148
wdrs:describedby
n5:doid.owl
Subject Item
_:vb50936872
rdf:type
owl:Restriction
owl:onProperty
n3:RO_0004019
owl:someValuesFrom
n3:SYMP_0000462
wdrs:describedby
n5:doid.owl