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Q47162422-02BE4ADD-BFEF-47C8-A710-3A3D716EB5FB
Q47162422-02BE4ADD-BFEF-47C8-A710-3A3D716EB5FB
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http://www.wikidata.org/entity/statement/Q47162422-02BE4ADD-BFEF-47C8-A710-3A3D716EB5FB
Clinical interpretation of copy number variants in the human genome.
P2860
Q47162422-02BE4ADD-BFEF-47C8-A710-3A3D716EB5FB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47162422-02BE4ADD-BFEF-47C8-A710-3A3D716EB5FB
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015eba657a058d1e6f3e2b7152cc65845f2cc1d0
P2860
A copy number variation map of the human genome