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Namespace Prefixes

Prefix	IRI
n5	http://linked.opendata.cz/resource/mesh/concept/
rdfs	http://www.w3.org/2000/01/rdf-schema#
rdf	http://www.w3.org/1999/02/22-rdf-syntax-ns#
n4	http://linked.opendata.cz/ontology/mesh/
owl	http://www.w3.org/2002/07/owl#
nci	http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
xsdh	http://www.w3.org/2001/XMLSchema#

Statements

Subject Item: nci:C4705
rdf:type: owl:Class
rdfs:label: Carney Complex
owl:equivalentClass: _:vb630957
nci:P106: Disease or Syndrome
nci:P108: Carney Complex
nci:P207: C0406810
nci:P325: <n0:ComplexDefinition xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:def-definition>A rare, inherited disorder marked by dark spots on the skin and tumors in the heart, endocrine glands, skin, and nerves. There are two types of Carney complex, which are caused by mutations (changes) in different genes.</n0:def-definition><n0:def-source>NCI-GLOSS</n0:def-source></n0:ComplexDefinition>
nci:P366: Carney_Complex
nci:P90: <n0:ComplexTerm xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:term-name>Carney syndrome</n0:term-name><n0:term-group>PT</n0:term-group><n0:term-source>NCI-GLOSS</n0:term-source><n0:source-code>CDR0000648572</n0:source-code></n0:ComplexTerm> <n0:ComplexTerm xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:term-name>Lentigines, Atrial Myxoma, Mucocutaneous Myoma, Blue Nevus Syndrome</n0:term-name><n0:term-group>SY</n0:term-group><n0:term-source>NCI</n0:term-source></n0:ComplexTerm> <n0:ComplexTerm xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:term-name>Carney's Syndrome</n0:term-name><n0:term-group>SY</n0:term-group><n0:term-source>NCI</n0:term-source></n0:ComplexTerm> <n0:ComplexTerm xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:term-name>Carney Complex</n0:term-name><n0:term-group>PT</n0:term-group><n0:term-source>NCI</n0:term-source></n0:ComplexTerm> <n0:ComplexTerm xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:term-name>LAMB</n0:term-name><n0:term-group>AB</n0:term-group><n0:term-source>NCI</n0:term-source></n0:ComplexTerm> <n0:ComplexTerm xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:term-name>Carney complex</n0:term-name><n0:term-group>PT</n0:term-group><n0:term-source>NCI-GLOSS</n0:term-source><n0:source-code>CDR0000597110</n0:source-code></n0:ComplexTerm> <n0:ComplexTerm xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:term-name>Atrial Myxoma with Lentigines</n0:term-name><n0:term-group>SY</n0:term-group><n0:term-source>NCI</n0:term-source></n0:ComplexTerm> <n0:ComplexTerm xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:term-name>CNC</n0:term-name><n0:term-group>AB</n0:term-group><n0:term-source>NCI</n0:term-source></n0:ComplexTerm> <n0:ComplexTerm xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:term-name>Carney Syndrome</n0:term-name><n0:term-group>SY</n0:term-group><n0:term-source>NCI</n0:term-source></n0:ComplexTerm> <n0:ComplexTerm xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:term-name>Nevi, Atrial Myxoma, Skin Myxoma, Ephelides Syndrome</n0:term-name><n0:term-group>SY</n0:term-group><n0:term-source>NCI</n0:term-source></n0:ComplexTerm>
nci:P97: <n0:ComplexDefinition xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:def-definition>An autosomal dominant disorder most often caused by mutations in the PRKAR1A gene. It is characterized by the presence of myxomas in the heart and skin, skin hyperpigmentation, increased endocrine activity and schwannomas.</n0:def-definition><n0:def-source>NCI</n0:def-source></n0:ComplexDefinition>
nci:code: C4705
n4:hasConcept: n5:M0528903

Subject Item: _:vb630957
rdf:type: owl:Class
owl:intersectionOf: _:vb730882

Subject Item: _:vb657745
rdf:type: owl:Restriction
owl:onProperty: nci:R174
owl:someValuesFrom: nci:C13212

Subject Item: _:vb657746
rdf:type: owl:Restriction
owl:onProperty: nci:R176
owl:someValuesFrom: nci:C97742

Subject Item: _:vb657747
rdf:type: owl:Restriction
owl:onProperty: nci:R116
owl:someValuesFrom: nci:C3506

Subject Item: _:vb657748
rdf:type: owl:Restriction
owl:onProperty: nci:R116
owl:someValuesFrom: nci:C3499

Subject Item: _:vb657749
rdf:type: owl:Restriction
owl:onProperty: nci:R116
owl:someValuesFrom: nci:C3329

Subject Item: _:vb657750
rdf:type: owl:Restriction
owl:onProperty: nci:R116
owl:someValuesFrom: nci:C3269

Subject Item: _:vb657751
rdf:type: owl:Restriction
owl:onProperty: nci:R116
owl:someValuesFrom: nci:C4672

Subject Item: _:vb657752
rdf:type: owl:Restriction
owl:onProperty: nci:R116
owl:someValuesFrom: nci:C4815

Subject Item: _:vb730882
rdf:first: nci:C3266
rdf:rest: _:vb754145

Subject Item: _:vb754145
rdf:first: _:vb657745
rdf:rest: _:vb754146

Subject Item: _:vb754146
rdf:first: _:vb657746
rdf:rest: _:vb754147

Subject Item: _:vb754147
rdf:first: _:vb657747
rdf:rest: _:vb754148

Subject Item: _:vb754148
rdf:first: _:vb657748
rdf:rest: _:vb754149

Subject Item: _:vb754149
rdf:first: _:vb657749
rdf:rest: _:vb754150

Subject Item: _:vb754150
rdf:first: _:vb657750
rdf:rest: _:vb754151

Subject Item: _:vb754151
rdf:first: _:vb657751
rdf:rest: _:vb754152

Subject Item: _:vb754152
rdf:first: _:vb657752
rdf:rest: rdf:nil