Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q9390341> ?p ?o }
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- Q9390341 subject Q6853266.
- Q9390341 subject Q6853484.
- Q9390341 subject Q7031586.
- Q9390341 abstract "Schwartz–Jampel syndrome (SJS) is a rare genetic disease caused by a mutation in the HSPG2 gene, which makes the protein perlecan, and causing osteochondrodysplasia associated with myotonia.Relationships between the disease and perlecan deficiency have been studied.".
- Q9390341 wikiPageWikiLink Q126540.
- Q9390341 wikiPageWikiLink Q1277793.
- Q9390341 wikiPageWikiLink Q14890110.
- Q9390341 wikiPageWikiLink Q200779.
- Q9390341 wikiPageWikiLink Q3251367.
- Q9390341 wikiPageWikiLink Q6853266.
- Q9390341 wikiPageWikiLink Q6853484.
- Q9390341 wikiPageWikiLink Q7031586.
- Q9390341 wikiPageWikiLink Q7720168.
- Q9390341 wikiPageWikiLink Q929833.
- Q9390341 comment "Schwartz–Jampel syndrome (SJS) is a rare genetic disease caused by a mutation in the HSPG2 gene, which makes the protein perlecan, and causing osteochondrodysplasia associated with myotonia.Relationships between the disease and perlecan deficiency have been studied.".
- Q9390341 label "Schwartz–Jampel syndrome".