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About:
clgr:
Variant_of_uncertain_significance
Property
Value
rdf:
type
owl:
NamedIndividual
Mutated gene
Genetic disease or disorder
Human genome project
rdfs:
label
Variant of uncertain significance
owl:
sameAs
dbr:
Variant_of_uncertain_significance
prov:
wasDerivedFrom
http://en.wikipedia.org/wiki/BRCA_mutation
http://en.wikipedia.org/wiki/Category:Mutated_genes
http://en.wikipedia.org/wiki/Category:Human_genome_projects
http://en.wikipedia.org/wiki/Category:Genetic_diseases_and_disorders
http://en.wikipedia.org/wiki/Category:Genetic_disorders_by_inheritance
http://en.wikipedia.org/wiki/Category:Genetic_disorders_by_mechanism
http://en.wikipedia.org/wiki/Category:Genetic_disorders_by_system
skos:
prefLabel
Variant of uncertain significance
skos:
altLabel
variant
Variant_of_uncertain_significance#Pathogenic
heterozygous pathogenic variant
pathogenic variants
variants of uncertain significance