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?:definition
  • A genetic finding indicating the presence of gene mutations in a sample that may be associated with cancer predisposition and are in located in genes other than BRCA1 and BRCA2.
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<http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.w3.org/2004/03/trix/rdfg-1/Graph>
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<http://xmlns.com/foaf/0.1/topic> Anon_0
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