Matches in Wikidata for { <http://www.wikidata.org/entity/Q51896097> ?p ?o ?g. }
- Q51896097 description "2007 nî lūn-bûn" @default.
- Q51896097 description "2007年の論文" @default.
- Q51896097 description "2007年学术文章" @default.
- Q51896097 description "2007年学术文章" @default.
- Q51896097 description "2007年学术文章" @default.
- Q51896097 description "2007年学术文章" @default.
- Q51896097 description "2007年学术文章" @default.
- Q51896097 description "2007年学术文章" @default.
- Q51896097 description "2007年學術文章" @default.
- Q51896097 description "2007年學術文章" @default.
- Q51896097 description "2007年學術文章" @default.
- Q51896097 description "2007年學術文章" @default.
- Q51896097 description "2007年學術文章" @default.
- Q51896097 description "2007년 논문" @default.
- Q51896097 description "article científic" @default.
- Q51896097 description "article scientific" @default.
- Q51896097 description "article scientifique" @default.
- Q51896097 description "articol științific" @default.
- Q51896097 description "articolo scientifico" @default.
- Q51896097 description "artigo científico" @default.
- Q51896097 description "artigo científico" @default.
- Q51896097 description "artigo científico" @default.
- Q51896097 description "artikel ilmiah" @default.
- Q51896097 description "artikull shkencor" @default.
- Q51896097 description "artikulong pang-agham" @default.
- Q51896097 description "artykuł naukowy" @default.
- Q51896097 description "artículo científico publicado en 2007" @default.
- Q51896097 description "artículu científicu" @default.
- Q51896097 description "bilimsel makale" @default.
- Q51896097 description "bài báo khoa học" @default.
- Q51896097 description "naučni članak" @default.
- Q51896097 description "scienca artikolo" @default.
- Q51896097 description "scientific article published on 13 December 2007" @default.
- Q51896097 description "scientific article published on 13 December 2007" @default.
- Q51896097 description "scientific article published on 13 December 2007" @default.
- Q51896097 description "teaduslik artikkel" @default.
- Q51896097 description "tieteellinen artikkeli" @default.
- Q51896097 description "tudományos cikk" @default.
- Q51896097 description "vedecký článok" @default.
- Q51896097 description "vetenskaplig artikel" @default.
- Q51896097 description "videnskabelig artikel" @default.
- Q51896097 description "vitenskapelig artikkel" @default.
- Q51896097 description "vitskapeleg artikkel" @default.
- Q51896097 description "vědecký článek" @default.
- Q51896097 description "wetenschappelijk artikel" @default.
- Q51896097 description "wissenschaftlicher Artikel" @default.
- Q51896097 description "επιστημονικό άρθρο" @default.
- Q51896097 description "мақолаи илмӣ" @default.
- Q51896097 description "наукова стаття, опублікована в грудні 2007" @default.
- Q51896097 description "научна статия" @default.
- Q51896097 description "научная статья" @default.
- Q51896097 description "научни чланак" @default.
- Q51896097 description "научни чланак" @default.
- Q51896097 description "מאמר מדעי" @default.
- Q51896097 description "مقالة علمية نشرت في 13 ديسمبر 2007" @default.
- Q51896097 description "১৩ ডিসেম্বর ২০০৭-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ" @default.
- Q51896097 description "บทความทางวิทยาศาสตร์" @default.
- Q51896097 description "სამეცნიერო სტატია" @default.
- Q51896097 name "Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration." @default.
- Q51896097 name "Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration." @default.
- Q51896097 type Item @default.
- Q51896097 label "Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration." @default.
- Q51896097 label "Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration." @default.
- Q51896097 prefLabel "Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration." @default.
- Q51896097 prefLabel "Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration." @default.
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