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Namespace Prefixes

PrefixIRI
n5https://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_0111545
rdf:type
owl:Class
rdfs:subClassOf
_:vb50945024 n2:DOID_0050736 n2:DOID_28
rdfs:label
familial male-limited precocious puberty
wdrs:describedby
n5:doid.owl
obo:id
DOID:0111545
obo:hasDbXref
OMIM:176410 UMLS_CUI:C0342549 MESH:D011629 SNOMEDCT_US_2021_09_01:237818003 UMLS_CUI:C1504412 MESH:C536961 ORDO:3000 GARD:4475
obo:hasExactSynonym
FMPP male-limited precocious puberty familial gonadotropin-independent male-limited sexual precocity testotoxicosis
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
An endocrine system disease characterized by onset in early childhood of accelerated growth, early development of secondary sexual characteristics, and reduced adult height in males only that has_material_basis_in heterozygous mutation in LHCGR on chromosome 2p16.3.
Subject Item
_:vb50945024
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000147
wdrs:describedby
n5:doid.owl