About: Cancer risk of heterozygotes with the NBN founder mutation

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An Entity of Type : http://linked.opendata.cz/ontology/domain/vavai/Vysledek, within Data Space : linked.opendata.cz associated with source document(s)

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rdf:type	skos:Concept http://linked.opendata.cz/ontology/domain/vavai/Vysledek
Description	Autosomálně recesivní (cs) The autosomal recessive chromosomal instability disorder Nijmegen breakage syndrome (NBS) is associated with increased risk of lymphoid malignancies. The autosomal recessive chromosomal instability disorder Nijmegen breakage syndrome (NBS) is associated with increased risk of lymphoid malignancies. (en)
Title	Cancer risk of heterozygotes with the NBN founder mutation Riziko (cs) Cancer risk of heterozygotes with the NBN founder mutation (en)
skos:prefLabel	Cancer risk of heterozygotes with the NBN founder mutation Riziko (cs) Cancer risk of heterozygotes with the NBN founder mutation (en)
skos:notation	RIV/00064203:_____/07:1508!RIV08-MZ0-00064203
http://linked.open.../vavai/riv/strany	1875-1880
http://linked.open...avai/riv/aktivita	P
http://linked.open...avai/riv/aktivity	P(NE6912), P(NH6439), P(NR7916)
http://linked.open...iv/cisloPeriodika	24
http://linked.open...vai/riv/dodaniDat	2008
http://linked.open...aciTvurceVysledku	Seeman, Pavel Seemanová, Eva Jarolím, Ladislav
http://linked.open.../riv/druhVysledku	J - Článek v odborném periodiku
http://linked.open...iv/duvernostUdaju	S - Úplné a pravdivé údaje nepodléhající ochraně podle zvláštních právních předpisů
http://linked.open...titaPredkladatele	Fakultní nemocnice v Motole
http://linked.open...dnocenehoVysledku	412579
http://linked.open...ai/riv/idVysledku	RIV/00064203:_____/07:1508
http://linked.open...riv/jazykVysledku	eng - angličtina
http://linked.open.../riv/klicovaSlova	NIJMEGEN-BREAKAGE-SYNDROME; ACUTE LYMPHOBLASTIC-LEUKEMIA; GERMLINE 657DEL5 MUTATION; SYNDROME GENE NBS1; BREAST-CANCER; CHROMOSOMAL INSTABILITY; ATAXIA-TELANGIECTASIA; CHILDHOOD; FREQUENCY; MALIGNANCIES (en)
http://linked.open.../riv/klicoveSlovo	BREAST-CANCER CHILDHOOD SYNDROME GENE NBS1 GERMLINE 657DEL5 MUTATION MALIGNANCIES CHROMOSOMAL INSTABILITY ATAXIA-TELANGIECTASIA FREQUENCY NIJMEGEN-BREAKAGE-SYNDROME ACUTE LYMPHOBLASTIC-LEUKEMIA
http://linked.open...odStatuVydavatele	US - Spojené státy americké
http://linked.open...ontrolniKodProRIV	[FEEEB6236AE2]
http://linked.open...i/riv/nazevZdroje	Journal of the national cancer institute
http://linked.open...in/vavai/riv/obor	FD
http://linked.open...ichTvurcuVysledku	3 (xsd:int)
http://linked.open...cetTvurcuVysledku	7 (xsd:int)
http://linked.open...vavai/riv/projekt	Molecular basis of congenital microcephaly - using molecular genetics and molecular cytogenetic methods for detection of etiology of different types of microcephaly and evaluation of clinical and genetic prognosis Submicroscopic chromosomal deletions - genotype-phenotype relation and a longitudinal study of patients Detection of Nijmegen Breakakge Syndrom (NBS) by DNA analysis among patients with malignancies
http://linked.open...UplatneniVysledku	2007
http://linked.open...v/svazekPeriodika	99
http://linked.open...iv/tvurceVysledku	Seemanová, Eva Seeman, Pavel Jarolím, Ladislav
issn	0027-8874
number of pages	6 (xsd:int)
is http://linked.open...avai/riv/vysledek of	Cancer risk of heterozygotes with the NBN founder mutation Cancer risk of heterozygotes with the NBN founder mutation Cancer risk of heterozygotes with the NBN founder mutation

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