SPARQL | HTML Microdata document
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Namespace Prefixes
Prefix IRI
rdfs http://www.w3.org/2000/01/rdf-schema#
rdf http://www.w3.org/1999/02/22-rdf-syntax-ns#
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:C46047
rdf:type
owl:Class
rdfs:label
CYP2D6*14 Allele
rdfs:subClassOf
_:vb655989
_:vb655990
_:vb655991
_:vb655992
_:vb655993
_:vb655994
nci:C26517
nci:P100
124030
nci:P102
NM_000106
nci:P106
Gene or Genome
nci:P108
CYP2D6*14 Allele
nci:P171
12089164
10064570
nci:P207
C1707210
nci:P366
CYP2D6_14_Allele
nci:P90
<n0:ComplexTerm xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:term-name>CYP2D6, G169R</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>CYP2D6*14 Allele</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>Cytochrome P450, Family 2, Subfamily D, Polypeptide 6*14 Allele</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>CYP2D6*14</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>CYP2D6, g.1758G>A</n0:term-name><n0:term-group>SY</n0:term-group><n0:term-source>NCI</n0:term-source></n0:ComplexTerm>
nci:P96
Cytochrome P450 2D6
nci:P97
<n0:ComplexDefinition xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:def-definition>Human CYP2D6*14 allele is located in the vicinity of 22q13.1 and is approximately 4 kb in length. This allele, a variant form of the CYP2D6 wild-type allele, encodes cytochrome P450 2D6*14 protein. The CYP2D6*14 allele exhibits a clinically-relevant SNP (g.1758G>A) that results in a G169R coding change. This alteration in protein sequence decreases the enzymatic activity of the cytochrome P450 2D6*14 protein.</n0:def-definition><n0:def-source>NCI</n0:def-source></n0:ComplexDefinition>
nci:P98
Ethnicity Association: Asian
nci:code
C46047
Subject Item _:vb655989
rdf:type
owl:Restriction
owl:onProperty
nci:R155
owl:someValuesFrom
nci:C13766
Subject Item _:vb655990
rdf:type
owl:Restriction
owl:onProperty
nci:R159
owl:someValuesFrom
nci:C45423
Subject Item _:vb655991
rdf:type
owl:Restriction
owl:onProperty
nci:R158
owl:someValuesFrom
nci:C26533
Subject Item _:vb655992
rdf:type
owl:Restriction
owl:onProperty
nci:R158
owl:someValuesFrom
nci:C26633
Subject Item _:vb655993
rdf:type
owl:Restriction
owl:onProperty
nci:R153
owl:someValuesFrom
nci:C45641
Subject Item _:vb655994
rdf:type
owl:Restriction
owl:onProperty
nci:R153
owl:someValuesFrom
nci:C18134