This HTML5 document contains 48 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

PrefixIRI
n6http://linked.opendata.cz/resource/mesh/concept/
rdfshttp://www.w3.org/2000/01/rdf-schema#
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
n5http://linked.opendata.cz/ontology/mesh/
owlhttp://www.w3.org/2002/07/owl#
ncihttp://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
xsdhhttp://www.w3.org/2001/XMLSchema#

Statements

Subject Item
nci:C2887
rdf:type
owl:Class
rdfs:label
Ataxia Telangiectasia Syndrome
owl:equivalentClass
_:vb629742
nci:P106
Disease or Syndrome
nci:P108
Ataxia Telangiectasia Syndrome
nci:P207
C0004135
nci:P325
<n0:ComplexDefinition xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:def-definition>A rare, inherited, progressive, degenerative disease of childhood that causes loss of muscle control, a weakened immune system, and an increased risk of cancer.</n0:def-definition><n0:def-source>NCI-GLOSS</n0:def-source></n0:ComplexDefinition>
nci:P366
Ataxia_Telangiectasia_Syndrome
nci:P90
<n0:ComplexTerm xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:term-name>ataxia-telangiectasia</n0:term-name><n0:term-group>PT</n0:term-group><n0:term-source>NCI-GLOSS</n0:term-source><n0:source-code>CDR0000270853</n0:source-code></n0:ComplexTerm> <n0:ComplexTerm xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:term-name>Ataxia Telangiectasia Syndrome</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>Louis-Bar 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>Ataxia Telangiectasia</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>Rare hereditary disease characterized by extreme sensitivity to ionizing radiation or radiomimetic drugs because of a defect in DNA repair. AT heterozygosity is estimated to occur in more than 2% of the U.S. population; heterozygotes exhibit increased radiation sensitivity and are at increased risk for several types of cancer. The normal version of the gene that is defective in AT appears to activate the p53-dependent response to DNA damage.</n0:def-definition><n0:def-source>NCI</n0:def-source></n0:ComplexDefinition>
nci:code
C2887
n5:hasConcept
n6:M0001898
Subject Item
_:vb629742
rdf:type
owl:Class
owl:intersectionOf
_:vb734807
Subject Item
_:vb647499
rdf:type
owl:Restriction
owl:onProperty
nci:R106
owl:someValuesFrom
nci:C40459
Subject Item
_:vb647500
rdf:type
owl:Restriction
owl:onProperty
nci:R176
owl:someValuesFrom
nci:C18583
Subject Item
_:vb647501
rdf:type
owl:Restriction
owl:onProperty
nci:R116
owl:someValuesFrom
nci:C3167
Subject Item
_:vb647502
rdf:type
owl:Restriction
owl:onProperty
nci:R116
owl:someValuesFrom
nci:C3211
Subject Item
_:vb647503
rdf:type
owl:Restriction
owl:onProperty
nci:R116
owl:someValuesFrom
nci:C4752
Subject Item
_:vb730685
rdf:first
nci:C84348
rdf:rest
_:vb748845
Subject Item
_:vb734804
rdf:first
nci:C7757
rdf:rest
_:vb730685
Subject Item
_:vb734807
rdf:first
nci:C27871
rdf:rest
_:vb734804
Subject Item
_:vb748845
rdf:first
_:vb647499
rdf:rest
_:vb748846
Subject Item
_:vb748846
rdf:first
_:vb647500
rdf:rest
_:vb748847
Subject Item
_:vb748847
rdf:first
_:vb647501
rdf:rest
_:vb748848
Subject Item
_:vb748848
rdf:first
_:vb647502
rdf:rest
_:vb748849
Subject Item
_:vb748849
rdf:first
_:vb647503
rdf:rest
rdf:nil