DEL17P13.1
http://dbpedia.org/resource/DEL17P13.1 an entity of type: Thing
Chromosome 17p13.1 deletion syndrome is a protein in humans that is encoded by the DEL17P13.1 gene.
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DEL17P13.1
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37885516
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1079525179
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Chromosome 17p13.1 deletion syndrome is a protein in humans that is encoded by the DEL17P13.1 gene.
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1094