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- Q18036731 abstract "Spartin is a protein that in humans is encoded by the SPG20 gene.This gene encodes a protein that contains a MIT (Microtubule Interacting and Trafficking molecule) domain. This protein may be involved in endosomal trafficking, microtubule dynamics, or both functions. Frameshift mutations associated with this gene cause autosomal recessive spastic paraplegia 20 (Troyer syndrome).Troyer syndrome (SPG20) is a complicated type of hereditary spastic paraplegias (HSPs). HSP is a category of neurological disorder characterized by spasticity and muscle weakness in the lower limbs.".
- Q18036731 entrezgene "23111".
- Q18036731 wikiPageExternalLink br.fcgi?book=gene&part=spg20.
- Q18036731 wikiPageWikiLink Q117060.
- Q18036731 wikiPageWikiLink Q1424895.
- Q18036731 wikiPageWikiLink Q1429154.
- Q18036731 wikiPageWikiLink Q1440688.
- Q18036731 wikiPageWikiLink Q1557686.
- Q18036731 wikiPageWikiLink Q1624054.
- Q18036731 wikiPageWikiLink Q183560.
- Q18036731 wikiPageWikiLink Q225957.
- Q18036731 wikiPageWikiLink Q3339235.
- Q18036731 wikiPageWikiLink Q517183.
- Q18036731 wikiPageWikiLink Q657516.
- Q18036731 wikiPageWikiLink Q7187.
- Q18036731 wikiPageWikiLink Q8054.
- Q18036731 type Biomolecule.
- Q18036731 type Protein.
- Q18036731 type Thing.
- Q18036731 type Q206229.
- Q18036731 type Q8054.
- Q18036731 comment "Spartin is a protein that in humans is encoded by the SPG20 gene.This gene encodes a protein that contains a MIT (Microtubule Interacting and Trafficking molecule) domain. This protein may be involved in endosomal trafficking, microtubule dynamics, or both functions. Frameshift mutations associated with this gene cause autosomal recessive spastic paraplegia 20 (Troyer syndrome).Troyer syndrome (SPG20) is a complicated type of hereditary spastic paraplegias (HSPs).".
- Q18036731 label "SPG20".