This HTML5 document contains 36 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

Prefix	IRI
n6	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#
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#

Statements

Subject Item

n2:DOID_3490

rdf:type

owl:Class

rdfs:subClassOf

_:vb50952002 _:vb50952003 n2:DOID_0050177 n2:DOID_0080690 _:vb50952004

rdfs:label

Noonan syndrome

rdfs:comment

OMIM mapping confirmed by DO. [SN].

wdrs:describedby

n6:doid.owl

obo:id

DOID:3490

obo:hasDbXref

GARD:10955 UMLS_CUI:C0028326 OMIM:PS163950 SNOMEDCT_US_2021_09_01:88327006 MESH:D009634 NCI:C34854 ICD10CM:Q87.19 ORDO:648

obo:hasExactSynonym

Turner's phenotype, karyotype normal

obo:hasOBONamespace

disease_ontology

obo:inSubset

n8:DO_FlyBase_slim n8:DO_rare_slim n8:NCIthesaurus

n2:IAO_0000115

A RASopathy that is characterized by mildly unusual facial features, short stature, heart defects, bleeding problems, skeletal malformations, and many other signs and symptoms.

Subject Item

_:vb50952002

rdf:type

owl:Restriction

owl:onProperty

n2:RO_0002452

owl:someValuesFrom

n2:SYMP_0000007

wdrs:describedby

n6:doid.owl

Subject Item

_:vb50952003

rdf:type

owl:Restriction

owl:onProperty

n2:RO_0002452

owl:someValuesFrom

n2:SYMP_0000568

wdrs:describedby

n6:doid.owl

Subject Item

_:vb50952004

rdf:type

owl:Restriction

owl:onProperty

n2:RO_0004019

owl:someValuesFrom

n2:SO_0000704

wdrs:describedby

n6:doid.owl