This HTML5 document contains 28 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

Prefix	IRI
n7	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#
skos	http://www.w3.org/2004/02/skos/core#
rdfs	http://www.w3.org/2000/01/rdf-schema#
obo	http://www.geneontology.org/formats/oboInOwl#
n9	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_1858

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_0050739 n2:DOID_225 _:vb50950230

rdfs:label

McCune Albright syndrome

rdfs:comment

OMIM mapping confirmed by DO. [SN].

skos:exactMatch

MESH:D005359

wdrs:describedby

n7:doid.owl

obo:id

DOID:1858

obo:hasAlternativeId

DOID:11345

obo:hasDbXref

NCI:C34610 GARD:6995 SNOMEDCT_US_2021_09_01:205508003 OMIM:174800 MESH:D005359 UMLS_CUI:C0016065 ICD10CM:Q78.1 ICD9CM:756.54

obo:hasExactSynonym

osteitis fibrosa disseminata fibrous dysplasia of bone polyostotic fibrous dysplasia

obo:hasOBONamespace

disease_ontology

obo:inSubset

n9:NCIthesaurus

n2:IAO_0000115

A syndrome that is characterized by polyostotic fibrous dysplasia, precocious puberty, and café-au-lait spots and has_material_basis_in spontaneous post zygotic missense mutation at ARG201 or Gln227 of the GNAS gene during embryogenesis.

Subject Item

_:vb50950230

rdf:type

owl:Restriction

owl:onProperty

n2:IDO_0000664

owl:someValuesFrom

n2:GENO_0000934

wdrs:describedby

n7:doid.owl