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Anualidad
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Research Project
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Continuant
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Entity
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Project
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Occurrent
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Specifically Dependent Continuant
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2018
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Grant
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Research Project
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RDF description of PCIN-2015-192-C02-01 - http://research.umh.es/vivo/pub/proyecto/PCIN2015192C0201
type: Document
rights: termsOfUse
date: 2026-08-01T20:50:43
publisher: PCIN-2015-192-C02-01

PCIN-2015-192-C02-01
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otricodigo: 2015/00335/001
description: Síndromes de discapacidad intelectual relacionados con alteraciones en la cromatina: Etiología molecular y terapia.
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geographic focus: national
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BFO_0000055: Principal Investigator on PCIN2015192C0201
date time interval: PCIN2015192C0201 date
relates: BARCO GUERRERO, ANGEL
relates: Principal Investigator on PCIN2015192C0201
referencia: PCIN-2015-192-C02-01
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codigo: PLANNAC-24291

Principal Investigator on PCIN2015192C0201
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BFO_0000054: PCIN-2015-192-C02-01
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BARCO GUERRERO, ANGEL
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Instituto de Neurociencias 2017
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includes: PCIN-2015-192-C02-01

Instituto de Neurociencias 2018
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type: ResearchReport
includes: PCIN-2015-192-C02-01