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An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • FANCG Gene
rdfs:subClassOf
OMIM_Number
  • 602956
Semantic_Type
  • Gene or Genome
Preferred_Name
  • FANCG Gene
UMLS_CUI
  • C1333532
Legacy_Concept_Name
  • FANCG_Gene
FULL_SYN
  • FANCGSYNCI
  • Fanconi Anemia, Complementation Group G GeneSYNCI
  • FANCG GenePTNCI
DEFINITION
  • This gene is involved in the maintenance of genomic integrity and nuclear signal transduction. Allelic variants of the gene are involved in Fanconi syndrome.NCI
code
  • C24385
is rdf:first of
is someValuesFrom of
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