This HTML5 document contains 73 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#
n4http://purl.obolibrary.org/obo/doid#
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_11983
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_0080014 n2:DOID_225 _:vb50948086 _:vb50948087
rdfs:label
Prader-Willi syndrome
rdfs:comment
OMIM mapping confirmed by DO. [SN].
wdrs:describedby
n6:doid.owl
obo:id
DOID:11983
obo:hasDbXref
SNOMEDCT_US_2021_09_01:205794007 ORDO:739 ICD9CM:759.81 MESH:D011218 UMLS_CUI:C0032897 NCI:C75463 OMIM:176270 ICD10CM:Q87.11 GARD:5575
obo:hasExactSynonym
Prader Willi syndrome
obo:hasOBONamespace
disease_ontology
obo:inSubset
n4:NCIthesaurus
n2:IAO_0000115
A chromosomal disease that is characterized by weak muscle tone, feeding difficulties, poor growth, and delayed development. Beginning in childhood, affected individuals develop an insatiable appetite, which leads to chronic overeating and obesity.
Subject Item
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owl:someValuesFrom
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wdrs:describedby
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Subject Item
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wdrs:describedby
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owl:onClass
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owl:minQualifiedCardinality
1
Subject Item
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wdrs:describedby
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Subject Item
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wdrs:describedby
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Subject Item
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Subject Item
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Subject Item
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