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- Q4645274 subject Q6853484.
- Q4645274 subject Q8482268.
- Q4645274 subject Q8803209.
- Q4645274 abstract "8p23.1 duplication syndrome is a rare genetic disorder caused by a duplication of a region from human chromosome 8. This duplication syndrome has an estimated prevalence of 1 in 64,000 births and is the reciprocal of the 8p23.1 deletion syndrome. The 8p23.1 duplication is associated with a variable phenotype including one or more of speech delay, developmental delay, mild dysmorphism, with prominent forehead and arched eyebrows, and congenital heart disease (CHD).".
- Q4645274 wikiPageExternalLink 85.
- Q4645274 wikiPageWikiLink Q104053.
- Q4645274 wikiPageWikiLink Q1142806.
- Q4645274 wikiPageWikiLink Q1269290.
- Q4645274 wikiPageWikiLink Q1360044.
- Q4645274 wikiPageWikiLink Q1472.
- Q4645274 wikiPageWikiLink Q1640386.
- Q4645274 wikiPageWikiLink Q16943522.
- Q4645274 wikiPageWikiLink Q179945.
- Q4645274 wikiPageWikiLink Q18033189.
- Q4645274 wikiPageWikiLink Q200779.
- Q4645274 wikiPageWikiLink Q2119430.
- Q4645274 wikiPageWikiLink Q2301465.
- Q4645274 wikiPageWikiLink Q3408238.
- Q4645274 wikiPageWikiLink Q4039110.
- Q4645274 wikiPageWikiLink Q412820.
- Q4645274 wikiPageWikiLink Q424523.
- Q4645274 wikiPageWikiLink Q572848.
- Q4645274 wikiPageWikiLink Q6853484.
- Q4645274 wikiPageWikiLink Q7049125.
- Q4645274 wikiPageWikiLink Q746284.
- Q4645274 wikiPageWikiLink Q83042.
- Q4645274 wikiPageWikiLink Q8482268.
- Q4645274 wikiPageWikiLink Q8803209.
- Q4645274 wikiPageWikiLink Q939364.
- Q4645274 name "8".
- Q4645274 type Disease.
- Q4645274 type Thing.
- Q4645274 type Q12136.
- Q4645274 comment "8p23.1 duplication syndrome is a rare genetic disorder caused by a duplication of a region from human chromosome 8. This duplication syndrome has an estimated prevalence of 1 in 64,000 births and is the reciprocal of the 8p23.1 deletion syndrome. The 8p23.1 duplication is associated with a variable phenotype including one or more of speech delay, developmental delay, mild dysmorphism, with prominent forehead and arched eyebrows, and congenital heart disease (CHD).".
- Q4645274 label "8p23.1 duplication syndrome".
- Q4645274 name "8p23.1 duplication syndrome".