This HTML5 document contains 56 embedded RDF statements represented using HTML+Microdata notation.

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

Namespace Prefixes

PrefixIRI
dctermshttp://purl.org/dc/terms/
n17http://linked.opendata.cz/resource/domain/vavai/projekt/
n14http://linked.opendata.cz/resource/domain/vavai/riv/tvurce/
n6http://linked.opendata.cz/ontology/domain/vavai/
n9http://linked.opendata.cz/resource/domain/vavai/zamer/
shttp://schema.org/
skoshttp://www.w3.org/2004/02/skos/core#
n3http://linked.opendata.cz/ontology/domain/vavai/riv/
n2http://linked.opendata.cz/resource/domain/vavai/vysledek/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
n13http://linked.opendata.cz/resource/domain/vavai/vysledek/RIV%2F00064203%3A_____%2F07%3A1587%21RIV08-MSM-00064203/
n5http://linked.opendata.cz/ontology/domain/vavai/riv/klicoveSlovo/
n18http://linked.opendata.cz/ontology/domain/vavai/riv/duvernostUdaju/
xsdhhttp://www.w3.org/2001/XMLSchema#
n16http://linked.opendata.cz/ontology/domain/vavai/riv/aktivita/
n12http://linked.opendata.cz/ontology/domain/vavai/riv/jazykVysledku/
n15http://linked.opendata.cz/ontology/domain/vavai/riv/druhVysledku/
n4http://linked.opendata.cz/ontology/domain/vavai/riv/obor/
n11http://reference.data.gov.uk/id/gregorian-year/

Statements

Subject Item
n2:RIV%2F00064203%3A_____%2F07%3A1587%21RIV08-MSM-00064203
rdf:type
n6:Vysledek skos:Concept
dcterms:description
X-linked agammaglobulinemia (XLA) is characterized by low levels of B-lymphocytes with early-onset, recurrent, microbial infections occasionally causing neurological symptoms. We observed an atypical clinical course of XLA, complicated since early childh X-linked agammaglobulinemia (XLA) is characterized by low levels of B-lymphocytes with early-onset, recurrent, microbial infections occasionally causing neurological symptoms. We observed an atypical clinical course of XLA, complicated since early childh Popis rozsáhlé delece na X chromozomu, která vysvětluje komplexní mnohočetná postižení u pacientů s Brutonovou agamagloublinémií
dcterms:title
Contiguous x-chromosome deletion syndrome encompassing the BTK, TIMM8A, TAF7L, and DRP2 genes Contiguous x-chromosome deletion syndrome encompassing the BTK, TIMM8A, TAF7L, and DRP2 genes Kontinuální delece zahrnující geny BTK, TIMM8A, TAF7L a DRP2
skos:prefLabel
Contiguous x-chromosome deletion syndrome encompassing the BTK, TIMM8A, TAF7L, and DRP2 genes Contiguous x-chromosome deletion syndrome encompassing the BTK, TIMM8A, TAF7L, and DRP2 genes Kontinuální delece zahrnující geny BTK, TIMM8A, TAF7L a DRP2
skos:notation
RIV/00064203:_____/07:1587!RIV08-MSM-00064203
n3:strany
640-646
n3:aktivita
n16:P n16:Z
n3:aktivity
P(1M0520), Z(MSM0021620812)
n3:cisloPeriodika
6
n3:dodaniDat
n11:2008
n3:domaciTvurceVysledku
n14:1987135 n14:5285593
n3:druhVysledku
n15:J
n3:duvernostUdaju
n18:S
n3:entitaPredkladatele
n13:predkladatel
n3:idSjednocenehoVysledku
414923
n3:idVysledku
RIV/00064203:_____/07:1587
n3:jazykVysledku
n12:eng
n3:klicovaSlova
X-linked agammaglobulinemia (XLA); Bruton tyrosine kinase (BTK); Mohr-Tranebjaerg syndrome; immunodeficiency; sensorineural deafness; recessive deafness syndrome; brutons tyrosine kinase; linked agammaglobulinemia; mental deficiency; ddp1/timm8a-timm13 complex; dystonia syndrome; ddp gene; mutation; family; expression
n3:klicoveSlovo
n5:brutons%20tyrosine%20kinase n5:mutation n5:Mohr-Tranebjaerg%20syndrome n5:Bruton%20tyrosine%20kinase%20%28BTK%29 n5:family n5:recessive%20deafness%20syndrome n5:ddp%20gene n5:ddp1%2Ftimm8a-timm13%20complex n5:dystonia%20syndrome n5:sensorineural%20deafness n5:linked%20agammaglobulinemia n5:X-linked%20agammaglobulinemia%20%28XLA%29 n5:immunodeficiency n5:expression n5:mental%20deficiency
n3:kodStatuVydavatele
US - Spojené státy americké
n3:kontrolniKodProRIV
[F124C3999CE4]
n3:nazevZdroje
Journal of Clinical Immunology
n3:obor
n4:EC
n3:pocetDomacichTvurcuVysledku
2
n3:pocetTvurcuVysledku
15
n3:projekt
n17:1M0520
n3:rokUplatneniVysledku
n11:2007
n3:svazekPeriodika
27
n3:tvurceVysledku
Janda, Aleš Šedivá, Anna
n3:zamer
n9:MSM0021620812
s:issn
0271-9142
s:numberOfPages
7