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@prefix rdfs: .
dbr:Variable_number_tandem_repeat rdfs:label "N\u00FAmero variable de repeticiones en t\u00E1ndem"@es ,
"Variable Number of Tandem Repeat"@it ,
"R\u00E9p\u00E9tition en tandem \u00E0 nombre variable"@fr ,
"Variable number tandem repeat"@en ,
"Variabel aantal tandemherhalingen"@nl ,
"\u53EF\u53D8\u6570\u76EE\u4E32\u8054\u91CD\u590D"@zh ;
rdfs:comment "Een variabel aantal tandemherhalingen of VNTR (variable number tandem repeat) is een reeks van 10 tot 100 opeenvolgende genetische herhalingen van een genetische sequentie, die 14 tot 100 basenparen lang kan zijn. Termen die ook naar dergelijke herhalingen verwijzen zijn minisatelliet en microsatelliet, dit zijn specifieke vormen van VNTR's."@nl ,
"En gen\u00E9tica molecular, el n\u00FAmero variable de repeticiones en t\u00E1ndem o VNTR (acr\u00F3nimo del ingl\u00E9s Variable Number of Tandem Repeats) son repeticiones de secuencias de 9 a 100 pares de bases que se utilizan como marcador molecular. El n\u00FAmero de repeticiones es variable pero en general es menor a 1000. Estos se pueden encontrar en muchos cromosomas y, a menudo, muestran variaciones en la longitud (n\u00FAmero de repeticiones) entre los individuos. Cada variante act\u00FAa como un alelo heredado, lo que permite su uso para la identificaci\u00F3n personal o parental. Su an\u00E1lisis es \u00FAtil en investigaci\u00F3n gen\u00E9tica y biol\u00F3gica, medicina forense y huellas gen\u00E9ticas"@es ,
"\u53EF\u53D8\u6570\u76EE\u4E32\u8054\u91CD\u590D\uFF08\u6216VNTR\uFF09\u662F\u57FA\u56E0\u7EC4\u4E2D\u7684\u4F4D\u7F6E\uFF0C\u5176\u4E2D\u88AB\u7EC4\u7EC7\u4E3A\u4E32\u8054\u91CD\u590D\u3002\u8FD9\u4E9B\u53EF\u4EE5\u5728\u8BB8\u591A\u67D3\u8272\u4F53\u4E0A\u627E\u5230\uFF0C\u5E76\u4E14\u7ECF\u5E38\u663E\u793A\u4E2A\u4F53\u4E4B\u95F4\u7684\u957F\u5EA6\u53D8\u5316\uFF08\u91CD\u590D\u7684\u6570\u91CF\uFF09\u3002 \u6BCF\u4E2A\u53D8\u4F53\u5145\u5F53\u9057\u4F20\u7B49\u4F4D\u57FA\u56E0\uFF0C\u5141\u8BB8\u5B83\u4EEC\u7528\u4E8E\u4E2A\u4EBA\u6216\u7236\u6BCD\u3002 \u4ED6\u4EEC\u7684\u5206\u6790\u5728\u9057\u4F20\u5B66\u548C\u751F\u7269\u5B66\u7814\u7A76\uFF0C\u6CD5\u533B\u5B66\u548CDNA\u6307\u7EB9\u5206\u6790\u4E2D\u5F88\u6709\u7528\u3002"@zh ,
"Une r\u00E9p\u00E9tition en tandem \u00E0 nombre variable (ou VNTR pour variable number tandem repeat en anglais) correspond \u00E0 un emplacement dans un g\u00E9nome o\u00F9 une courte s\u00E9quence nucl\u00E9otidique est organis\u00E9e comme une r\u00E9p\u00E9tition en tandem. On peut les trouver sur de nombreux chromosomes et elles montrent souvent des variations de longueur (nombre de r\u00E9p\u00E9titions) d'un individu \u00E0 l'autre. Chaque variante agit comme un all\u00E8le h\u00E9rit\u00E9, ce qui permet de les utiliser pour une identification personnelle ou parentale. Leur analyse est utile dans la recherche g\u00E9n\u00E9tique et biologique, la criminalistique et les empreintes digitales d'ADN."@fr ,
"In biologia molecolare, la sigla VNTR (dall'inglese Variable Number of Tandem Repeats, numero variabile di ripetizioni in tandem) viene utilizzata per indicare polimorfismi del DNA in cui la differenza tra le diverse varianti non \u00E8 data da un cambio nucleotidico (come \u00E8 invece per i SNP - polimorfismi a singolo nucleotide - o gli RFLP) ma dalla ripetizione in tandem di specifiche sequenze nucleotidiche. Le sequenze ripetute del nostro genoma sono diverse e di diversa origine e rappresentano circa il 44% del nostro DNA, quelle ripetute in tandem sono caratterizzate dal fatto che le unit\u00E0 di ripetizione si trovano adiacenti l'una all'altra mentre quelle che si definiscono intersperse possono anche trovarsi in punti distanti tra loro (ad esempio i retrotrasposoni)."@it ,
"A variable number tandem repeat (or VNTR) is a location in a genome where a short nucleotide sequence is organized as a tandem repeat. These can be found on many chromosomes, and often show variations in length (number of repeats) among individuals. Each variant acts as an inherited allele, allowing them to be used for personal or parental identification. Their analysis is useful in genetics and biology research, forensics, and DNA fingerprinting."@en ;
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,
,
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dbr:Variable_number_tandem_repeat dcterms:subject dbc:Repetitive_DNA_sequences ;
dbo:abstract "Une r\u00E9p\u00E9tition en tandem \u00E0 nombre variable (ou VNTR pour variable number tandem repeat en anglais) correspond \u00E0 un emplacement dans un g\u00E9nome o\u00F9 une courte s\u00E9quence nucl\u00E9otidique est organis\u00E9e comme une r\u00E9p\u00E9tition en tandem. On peut les trouver sur de nombreux chromosomes et elles montrent souvent des variations de longueur (nombre de r\u00E9p\u00E9titions) d'un individu \u00E0 l'autre. Chaque variante agit comme un all\u00E8le h\u00E9rit\u00E9, ce qui permet de les utiliser pour une identification personnelle ou parentale. Leur analyse est utile dans la recherche g\u00E9n\u00E9tique et biologique, la criminalistique et les empreintes digitales d'ADN."@fr ,
"In biologia molecolare, la sigla VNTR (dall'inglese Variable Number of Tandem Repeats, numero variabile di ripetizioni in tandem) viene utilizzata per indicare polimorfismi del DNA in cui la differenza tra le diverse varianti non \u00E8 data da un cambio nucleotidico (come \u00E8 invece per i SNP - polimorfismi a singolo nucleotide - o gli RFLP) ma dalla ripetizione in tandem di specifiche sequenze nucleotidiche. Le sequenze ripetute del nostro genoma sono diverse e di diversa origine e rappresentano circa il 44% del nostro DNA, quelle ripetute in tandem sono caratterizzate dal fatto che le unit\u00E0 di ripetizione si trovano adiacenti l'una all'altra mentre quelle che si definiscono intersperse possono anche trovarsi in punti distanti tra loro (ad esempio i retrotrasposoni)."@it ,
"\u53EF\u53D8\u6570\u76EE\u4E32\u8054\u91CD\u590D\uFF08\u6216VNTR\uFF09\u662F\u57FA\u56E0\u7EC4\u4E2D\u7684\u4F4D\u7F6E\uFF0C\u5176\u4E2D\u88AB\u7EC4\u7EC7\u4E3A\u4E32\u8054\u91CD\u590D\u3002\u8FD9\u4E9B\u53EF\u4EE5\u5728\u8BB8\u591A\u67D3\u8272\u4F53\u4E0A\u627E\u5230\uFF0C\u5E76\u4E14\u7ECF\u5E38\u663E\u793A\u4E2A\u4F53\u4E4B\u95F4\u7684\u957F\u5EA6\u53D8\u5316\uFF08\u91CD\u590D\u7684\u6570\u91CF\uFF09\u3002 \u6BCF\u4E2A\u53D8\u4F53\u5145\u5F53\u9057\u4F20\u7B49\u4F4D\u57FA\u56E0\uFF0C\u5141\u8BB8\u5B83\u4EEC\u7528\u4E8E\u4E2A\u4EBA\u6216\u7236\u6BCD\u3002 \u4ED6\u4EEC\u7684\u5206\u6790\u5728\u9057\u4F20\u5B66\u548C\u751F\u7269\u5B66\u7814\u7A76\uFF0C\u6CD5\u533B\u5B66\u548CDNA\u6307\u7EB9\u5206\u6790\u4E2D\u5F88\u6709\u7528\u3002"@zh ,
"Een variabel aantal tandemherhalingen of VNTR (variable number tandem repeat) is een reeks van 10 tot 100 opeenvolgende genetische herhalingen van een genetische sequentie, die 14 tot 100 basenparen lang kan zijn. Termen die ook naar dergelijke herhalingen verwijzen zijn minisatelliet en microsatelliet, dit zijn specifieke vormen van VNTR's. Afhankelijk van welke repeats er plaatsvinden, kunnen ze aanleiding geven tot ziekten. Dit is dan een gevolg van mutaties tijdens een translatieproces. Een voorbeeld is een herhaling van de reeks cytosine\u2013adenine\u2013guanine, een zogenaamde CAG-repeat. Deze wordt gelinkt aan de ziekte van Huntington, prostaatkanker en de ziekte van Kennedy. VNTR's kunnen gebruikt worden voor onderzoek van populatiegenetica aan de hand van polymorfe loci: Zo is er een hexamorfe VNTR van 86 basenparen in intron 2 van de IL-1 receptorantagonist op chromosoom 2. Door de verschillende allelen uit te knippen met restrictie-enzymen en te visualiseren met gel-elektroforese, ontstaat een karakteristieke 'vingerafdruk'."@nl ,
"En gen\u00E9tica molecular, el n\u00FAmero variable de repeticiones en t\u00E1ndem o VNTR (acr\u00F3nimo del ingl\u00E9s Variable Number of Tandem Repeats) son repeticiones de secuencias de 9 a 100 pares de bases que se utilizan como marcador molecular. El n\u00FAmero de repeticiones es variable pero en general es menor a 1000. Estos se pueden encontrar en muchos cromosomas y, a menudo, muestran variaciones en la longitud (n\u00FAmero de repeticiones) entre los individuos. Cada variante act\u00FAa como un alelo heredado, lo que permite su uso para la identificaci\u00F3n personal o parental. Su an\u00E1lisis es \u00FAtil en investigaci\u00F3n gen\u00E9tica y biol\u00F3gica, medicina forense y huellas gen\u00E9ticas"@es ,
"A variable number tandem repeat (or VNTR) is a location in a genome where a short nucleotide sequence is organized as a tandem repeat. These can be found on many chromosomes, and often show variations in length (number of repeats) among individuals. Each variant acts as an inherited allele, allowing them to be used for personal or parental identification. Their analysis is useful in genetics and biology research, forensics, and DNA fingerprinting."@en ;
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