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About:
Molecular diagnosis of Rett syndrome: Detection of the prevalent mutation in MeCP2 gene in Czech and Slovak patients
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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)
Type:
skos:Concept
http://linked.opendata.cz/ontology/domain/vavai/Vysledek
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rdf:type
skos:Concept
http://linked.opendata.cz/ontology/domain/vavai/Vysledek
Description
Rett syndrome
Rett syndrome
(en)
Title
Molecular diagnosis of Rett syndrome: Detection of the prevalent mutation in MeCP2 gene in Czech and Slovak patients
Molecular diagnosis of Rett syndrome: Detection of the prevalent mutation in MeCP2 gene in Czech and Slovak patients
(en)
skos:prefLabel
Molecular diagnosis of Rett syndrome: Detection of the prevalent mutation in MeCP2 gene in Czech and Slovak patients
Molecular diagnosis of Rett syndrome: Detection of the prevalent mutation in MeCP2 gene in Czech and Slovak patients
(en)
skos:notation
RIV/00064165:_____/01:00000372!RIV/2002/GA0/L38002/N
http://linked.open.../vavai/riv/strany
281;281
http://linked.open...avai/riv/aktivita
P
http://linked.open...avai/riv/aktivity
P(GA201/00/P068), P(GA302/99/0648), P(GP301/01/P068)
http://linked.open...iv/cisloPeriodika
Suppl. 1
http://linked.open...vai/riv/dodaniDat
2002
http://linked.open...aciTvurceVysledku
Rosipal, Robert
Martásek, Pavel
Zeman, Jiří
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
Všeobecná fakultní nemocnice v Praze / (nerozlišená součást)
http://linked.open...dnocenehoVysledku
687565
http://linked.open...ai/riv/idVysledku
RIV/00064165:_____/01:00000372
http://linked.open...riv/jazykVysledku
eng - angličtina
http://linked.open.../riv/klicovaSlova
Molecular;diagnosis;syndrome;Detection;prevalent;mutation;MeCP2;Czech;Slovak;patients
(en)
http://linked.open.../riv/klicoveSlovo
patients
Czech
diagnosis
Detection
Slovak
Molecular
mutation
MeCP2
syndrome
prevalent
http://linked.open...odStatuVydavatele
GB - Spojené království Velké Británie a Severního Irska
http://linked.open...ontrolniKodProRIV
[D72B5A52A1F7]
http://linked.open...i/riv/nazevZdroje
European Journal of Human Genetics
http://linked.open...in/vavai/riv/obor
FL
http://linked.open...ichTvurcuVysledku
3
(
xsd:int
)
http://linked.open...cetTvurcuVysledku
5
(
xsd:int
)
http://linked.open...ocetUcastnikuAkce
0
(
xsd:int
)
http://linked.open...nichUcastnikuAkce
0
(
xsd:int
)
http://linked.open...vavai/riv/projekt
Structure of standard invariant operators for parabolic geometries
Genetics and functional manifestation of heteroplasmic mt DNA mutations
Molecular analysis of the MeCP2 gene in patients with Rett syndrome
http://linked.open...UplatneniVysledku
2001
http://linked.open...v/svazekPeriodika
9
http://linked.open...iv/tvurceVysledku
Zeman, Jiří
Martásek, Pavel
Rosipal, Robert
issn
1018-4813
number of pages
1
(
xsd:int
)
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