Matches in Wikidata for { <http://www.wikidata.org/entity/Q40920042> ?p ?o ?g. }
- Q40920042 description "1999 nî lūn-bûn" @default.
- Q40920042 description "1999年の論文" @default.
- Q40920042 description "1999年学术文章" @default.
- Q40920042 description "1999年学术文章" @default.
- Q40920042 description "1999年学术文章" @default.
- Q40920042 description "1999年学术文章" @default.
- Q40920042 description "1999年学术文章" @default.
- Q40920042 description "1999年學術文章" @default.
- Q40920042 description "1999年學術文章" @default.
- Q40920042 description "1999年學術文章" @default.
- Q40920042 description "1999年學術文章" @default.
- Q40920042 description "1999年學術文章" @default.
- Q40920042 description "1999年學術文章" @default.
- Q40920042 description "1999년 논문" @default.
- Q40920042 description "article científic" @default.
- Q40920042 description "article scientific" @default.
- Q40920042 description "article scientifique (publié 1999)" @default.
- Q40920042 description "articol științific" @default.
- Q40920042 description "articolo scientifico" @default.
- Q40920042 description "artigo científico (publicado na 1999)" @default.
- Q40920042 description "artigo científico (publicado na 1999)" @default.
- Q40920042 description "artigo científico" @default.
- Q40920042 description "artikull shkencor" @default.
- Q40920042 description "artikulong pang-agham" @default.
- Q40920042 description "artykuł naukowy" @default.
- Q40920042 description "artículo científico publicado en 1999" @default.
- Q40920042 description "artículu científicu espublizáu en 1999" @default.
- Q40920042 description "bilimsel makale" @default.
- Q40920042 description "bài báo khoa học" @default.
- Q40920042 description "mokslinis straipsnis" @default.
- Q40920042 description "naučni članak" @default.
- Q40920042 description "scienca artikolo" @default.
- Q40920042 description "scientific article" @default.
- Q40920042 description "teaduslik artikkel" @default.
- Q40920042 description "tieteellinen artikkeli" @default.
- Q40920042 description "tudományos cikk" @default.
- Q40920042 description "vedecký článok" @default.
- Q40920042 description "vetenskaplig artikel" @default.
- Q40920042 description "videnskabelig artikel (udgivet 1999)" @default.
- Q40920042 description "vitenskapelig artikkel" @default.
- Q40920042 description "vitskapeleg artikkel" @default.
- Q40920042 description "vědecký článek" @default.
- Q40920042 description "wetenschappelijk artikel" @default.
- Q40920042 description "wissenschaftlicher Artikel" @default.
- Q40920042 description "επιστημονικό άρθρο" @default.
- Q40920042 description "мақолаи илмӣ" @default.
- Q40920042 description "мақолаи илмӣ" @default.
- Q40920042 description "наукова стаття, опублікована в листопаді 1999" @default.
- Q40920042 description "научна статия" @default.
- Q40920042 description "научная статья" @default.
- Q40920042 description "научни чланак" @default.
- Q40920042 description "научни чланак" @default.
- Q40920042 description "գիտական հոդված" @default.
- Q40920042 description "מאמר מדעי" @default.
- Q40920042 description "سائنسی مضمون" @default.
- Q40920042 description "مقالة علمية نشرت في نوفمبر 1999" @default.
- Q40920042 description "مقالهٔ علمی" @default.
- Q40920042 description "১৯৯৯-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ" @default.
- Q40920042 description "บทความทางวิทยาศาสตร์" @default.
- Q40920042 description "სამეცნიერო სტატია" @default.
- Q40920042 name "Expression analysis of four endoglin missense mutations suggests that haploinsufficiency is the predominant mechanism for hereditary hemorrhagic telangiectasia type 1." @default.
- Q40920042 type Item @default.
- Q40920042 label "Expression analysis of four endoglin missense mutations suggests that haploinsufficiency is the predominant mechanism for hereditary hemorrhagic telangiectasia type 1." @default.
- Q40920042 prefLabel "Expression analysis of four endoglin missense mutations suggests that haploinsufficiency is the predominant mechanism for hereditary hemorrhagic telangiectasia type 1." @default.
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- Q40920042 P356 8.12.2171 @default.
- Q40920042 P698 10545596 @default.
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- Q40920042 P1476 "Expression analysis of four endoglin missense mutations suggests that haploinsufficiency is the predominant mechanism for hereditary hemorrhagic telangiectasia type 1." @default.
- Q40920042 P2093 "D A Marchuk" @default.
- Q40920042 P2093 "M Letarte" @default.
- Q40920042 P2093 "N Pece-Barbara" @default.
- Q40920042 P2093 "S Vera" @default.
- Q40920042 P2093 "U Cymerman" @default.
- Q40920042 P2860 Q28245861 @default.
- Q40920042 P304 "2171-2181" @default.
- Q40920042 P31 Q13442814 @default.
- Q40920042 P356 "10.1093/HMG/8.12.2171" @default.
- Q40920042 P433 "12" @default.
- Q40920042 P478 "8" @default.
- Q40920042 P577 "1999-11-01T00:00:00Z" @default.
- Q40920042 P5875 "12754429" @default.