This HTML5 document contains 43 embedded RDF statements represented using HTML+Microdata notation.

The embedded RDF content will be recognized by any processor of HTML5 Microdata.

Namespace Prefixes

PrefixIRI
n16http://linked.opendata.cz/ontology/domain/vavai/cep/typPojektu/
n18http://linked.opendata.cz/ontology/domain/vavai/cep/zivotniCyklusProjektu/
n13http://linked.opendata.cz/ontology/domain/vavai/cep/druhSouteze/
n9http://linked.opendata.cz/ontology/domain/vavai/cep/hodnoceniProjektu/
dctermshttp://purl.org/dc/terms/
n2http://linked.opendata.cz/resource/domain/vavai/projekt/
n15http://linked.opendata.cz/resource/domain/vavai/subjekt/
n20http://linked.opendata.cz/resource/domain/vavai/projekt/7E09041/
n8http://linked.opendata.cz/resource/domain/vavai/cep/prideleniPodpory/
n6http://linked.opendata.cz/ontology/domain/vavai/cep/kategorie/
n3http://linked.opendata.cz/ontology/domain/vavai/
n17http://linked.opendata.cz/ontology/domain/vavai/cep/duvernostUdaju/
rdfshttp://www.w3.org/2000/01/rdf-schema#
skoshttp://www.w3.org/2004/02/skos/core#
n22http://linked.opendata.cz/ontology/domain/vavai/cep/fazeProjektu/
n7http://linked.opendata.cz/ontology/domain/vavai/cep/obor/
n21http://linked.opendata.cz/ontology/domain/vavai/cep/statusZobrazovaneFaze/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
xsdhhttp://www.w3.org/2001/XMLSchema#
n5http://linked.opendata.cz/ontology/domain/vavai/cep/
n11http://linked.opendata.cz/resource/domain/vavai/cep/vyzva/
n19http://linked.opendata.cz/resource/domain/vavai/aktivita/
n14http://reference.data.gov.uk/id/gregorian-year/

Statements

Subject Item
n2:7E09041
rdf:type
n3:Projekt
rdfs:seeAlso
http://www.isvav.cz/projectDetail.do?rowId=7E09041
dcterms:description
Mental retardation (MR) is a highly heterogeneous disorder and is of genetic origin in about 50% of the cases. Despite recent progress in research the causes and the pathophysiology of MR remains obscure. It is essential to investigate this in order to develop future diagnostic and therapeutic strategies. The overall goal of this proposal is to establish an interdisciplinary Eastern Europe and Central Asia (EECA) consortium of experts with a joint programme of activities to generate knowledge about MR and the structure and dynamics of the brain as such. This project will be the first to study in depth the prevalence and incidence of MR in EECA. The objectives of the CHERISH project are to: - develop a standardized approach for MR diagnosis through clinical workshops and courses; - create a large data-base of patients with clinically well defined MR, both syndromic and non-syndromic; - identify cryptic genomic rearrangements through molecular cytogenetic analysis; - sequence MR genes and analyse the m Mental retardation (MR) is a highly heterogeneous disorder and is of genetic origin in about 50% of the cases. Despite recent progress in research the causes and the pathophysiology of MR remains obscure. It is essential to investigate this in order to develop future diagnostic and therapeutic strategies. The overall goal of this proposal is to establish an interdisciplinary Eastern Europe and Central Asia (EECA) consortium of experts with a joint programme of activities to generate knowledge about MR and the structure and dynamics of the brain as such. This project will be the first to study in depth the prevalence and incidence of MR in EECA. The objectives of the CHERISH project are to: - develop a standardized approach for MR diagnosis through clinical workshops and courses; - create a large data-base of patients with clinically well defined MR, both syndromic and non-syndromic; - identify cryptic genomic rearrangements through molecular cytogenetic analysis; - sequence MR genes and analyse the m
dcterms:title
Improving Diagnoses of Mental Retardation in Children in Eastern Europe and Central Asia through Genetic Characterisation and Bioinformatics/Statistics Improving Diagnoses of Mental Retardation in Children in Eastern Europe and Central Asia through Genetic Characterisation and Bioinformatics/Statistics
skos:notation
7E09041
n5:aktivita
n19:7E
n5:celkovaStatniPodpora
n20:celkovaStatniPodpora
n5:celkoveNaklady
n20:celkoveNaklady
n5:datumDodatniDoRIV
2013-06-28+02:00
n5:druhSouteze
n13:RP
n5:duvernostUdaju
n17:S
n5:fazeProjektu
n22:92902020
n5:hlavniObor
n7:EB
n5:hodnoceniProjektu
n9:U
n5:kategorie
n6:ZV
n5:klicovaSlova
Mental retardation; Eastern Europe; Central Asia; Genetics; Genomics; Children; Adolescence
n5:partnetrHlavni
n15:orjk%3A11130
n5:pocetKoordinujicichPrijemcu
0
n5:pocetPrijemcu
1
n5:pocetSpoluPrijemcu
0
n5:pocetVysledkuRIV
0
n5:pocetZverejnenychVysledkuVRIV
0
n5:prideleniPodpory
n8:1086%2F2011-321
n5:sberDatUcastniciPoslednihoRoku
n14:2012
n5:sberDatUdajeProjZameru
n14:2013
n5:statusZobrazovaneFaze
n21:DUU
n5:typPojektu
n16:P
n5:ukonceniReseni
2012-01-31+01:00
n5:vedlejsiObor
n7:FG n7:FP
n5:zahajeniReseni
2009-02-01+01:00
n5:zhodnoceni+vysledku+projektu+dodavatelem
Hodnocení výsledků řešení ministerstvo neprovádí, neboť podmínkou podpory je, že uchazeč byl vybrán mezinárodním poskytovatelem v souladu s pravidly příslušného programu. Projekt je hodnocen až po jeho schválení mezinárodním poskytovatelem. Following the condition that the candidate of financial contribution was evaluated and afterwards selected by international provider in accordance with the rules of the program the Ministry of Education, Youth ans Sports does not realize the evaluation of project results. The project is evaluated only after its approval by an international provider.
n5:zivotniCyklusProjektu
n18:ZBBKU
n5:vyzva
n11:FP7-Health-2009-two-stage
n5:klicoveSlovo
Genomics Mental retardation Eastern Europe Children Central Asia Genetics