FRINK Linked Data Fragments server

Matches in Wikidata for { <http://www.wikidata.org/entity/Q52641748> ?p ?o ?g. }

• Q52641748 description "2018 nî lūn-bûn" @default.
• Q52641748 description "2018年の論文" @default.
• Q52641748 description "2018年学术文章" @default.
• Q52641748 description "2018年学术文章" @default.
• Q52641748 description "2018年学术文章" @default.
• Q52641748 description "2018年学术文章" @default.
• Q52641748 description "2018年学术文章" @default.
• Q52641748 description "2018年学术文章" @default.
• Q52641748 description "2018年學術文章" @default.
• Q52641748 description "2018年學術文章" @default.
• Q52641748 description "2018年學術文章" @default.
• Q52641748 description "2018年學術文章" @default.
• Q52641748 description "2018年學術文章" @default.
• Q52641748 description "2018년 논문" @default.
• Q52641748 description "article científic" @default.
• Q52641748 description "article scientific" @default.
• Q52641748 description "article scientifique" @default.
• Q52641748 description "articol științific" @default.
• Q52641748 description "articolo scientifico" @default.
• Q52641748 description "artigo científico" @default.
• Q52641748 description "artigo científico" @default.
• Q52641748 description "artigo científico" @default.
• Q52641748 description "artikel ilmiah" @default.
• Q52641748 description "artikull shkencor" @default.
• Q52641748 description "artikulong pang-agham" @default.
• Q52641748 description "artykuł naukowy" @default.
• Q52641748 description "artículo científico publicado en 2018" @default.
• Q52641748 description "artículu científicu" @default.
• Q52641748 description "bilimsel makale" @default.
• Q52641748 description "bài báo khoa học" @default.
• Q52641748 description "naučni članak" @default.
• Q52641748 description "scienca artikolo" @default.
• Q52641748 description "scientific article published on 22 March 2018" @default.
• Q52641748 description "scientific article published on 22 March 2018" @default.
• Q52641748 description "scientific article published on 22 March 2018" @default.
• Q52641748 description "teaduslik artikkel" @default.
• Q52641748 description "tieteellinen artikkeli" @default.
• Q52641748 description "tudományos cikk" @default.
• Q52641748 description "vedecký článok" @default.
• Q52641748 description "vetenskaplig artikel" @default.
• Q52641748 description "videnskabelig artikel" @default.
• Q52641748 description "vitenskapelig artikkel" @default.
• Q52641748 description "vitskapeleg artikkel" @default.
• Q52641748 description "vědecký článek" @default.
• Q52641748 description "wetenschappelijk artikel" @default.
• Q52641748 description "wissenschaftlicher Artikel" @default.
• Q52641748 description "επιστημονικό άρθρο" @default.
• Q52641748 description "мақолаи илмӣ" @default.
• Q52641748 description "наукова стаття, опублікована в березні 2018" @default.
• Q52641748 description "научна статия" @default.
• Q52641748 description "научная статья" @default.
• Q52641748 description "научни чланак" @default.
• Q52641748 description "научни чланак" @default.
• Q52641748 description "מאמר מדעי" @default.
• Q52641748 description "مقالة علمية نشرت في 22 مارس 2018" @default.
• Q52641748 description "২২ মার্চ ২০১৮-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ" @default.
• Q52641748 description "บทความทางวิทยาศาสตร์" @default.
• Q52641748 description "სამეცნიერო სტატია" @default.
• Q52641748 name "A complete, homozygous CRX deletion causing nullizygosity is a new genetic mechanism for Leber congenital amaurosis." @default.
• Q52641748 name "A complete, homozygous CRX deletion causing nullizygosity is a new genetic mechanism for Leber congenital amaurosis." @default.
• Q52641748 type Item @default.
• Q52641748 label "A complete, homozygous CRX deletion causing nullizygosity is a new genetic mechanism for Leber congenital amaurosis." @default.
• Q52641748 label "A complete, homozygous CRX deletion causing nullizygosity is a new genetic mechanism for Leber congenital amaurosis." @default.
• Q52641748 prefLabel "A complete, homozygous CRX deletion causing nullizygosity is a new genetic mechanism for Leber congenital amaurosis." @default.
• Q52641748 prefLabel "A complete, homozygous CRX deletion causing nullizygosity is a new genetic mechanism for Leber congenital amaurosis." @default.
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• Q52641748 P698 29568065 @default.
• Q52641748 P1433 Q2261792 @default.
• Q52641748 P1476 "A complete, homozygous CRX deletion causing nullizygosity is a new genetic mechanism for Leber congenital amaurosis." @default.

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