About: DEL17P13.1

An Entity of Type: protein, from Named Graph: http://dbpedia.org, within Data Space: dbpedia.org

Chromosome 17p13.1 deletion syndrome is a protein in humans that is encoded by the DEL17P13.1 gene.

Property	Value
dbo:abstract	Chromosome 17p13.1 deletion syndrome is a protein in humans that is encoded by the DEL17P13.1 gene. (en)
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rdfs:comment	Chromosome 17p13.1 deletion syndrome is a protein in humans that is encoded by the DEL17P13.1 gene. (en)
rdfs:label	DEL17P13.1 (en)
owl:sameAs	freebase:DEL17P13.1 yago-res:DEL17P13.1 wikidata:DEL17P13.1 http://bs.dbpedia.org/resource/DEL17P13.1 https://global.dbpedia.org/id/yz8f
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