Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/SPG20> ?p ?o }
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- SPG20 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.".
- SPG20 entrezgene "23111".
- SPG20 wikiPageExternalLink br.fcgi?book=gene&part=spg20.
- SPG20 wikiPageID "14873964".
- SPG20 wikiPageLength "9826".
- SPG20 wikiPageOutDegree "17".
- SPG20 wikiPageRevisionID "679041118".
- SPG20 wikiPageWikiLink Clonus.
- SPG20 wikiPageWikiLink Dysarthria.
- SPG20 wikiPageWikiLink Dysmetria.
- SPG20 wikiPageWikiLink Frameshift_mutation.
- SPG20 wikiPageWikiLink Frameshift_mutations.
- SPG20 wikiPageWikiLink Gene.
- SPG20 wikiPageWikiLink Hereditary_spastic_paraplegia.
- SPG20 wikiPageWikiLink Hyperreflexia.
- SPG20 wikiPageWikiLink Intellectual_disability.
- SPG20 wikiPageWikiLink Mental_retardation.
- SPG20 wikiPageWikiLink Muscle_atrophy.
- SPG20 wikiPageWikiLink Neurological_disorder.
- SPG20 wikiPageWikiLink Pes_cavus.
- SPG20 wikiPageWikiLink Protein.
- SPG20 wikiPageWikiLink Spastic_paraplegia.
- SPG20 wikiPageWikiLink Spasticity.
- SPG20 wikiPageWikiLinkText "SPG20".
- SPG20 hasPhotoCollection SPG20.
- SPG20 requireManualInspection "no".
- SPG20 summaryText "This gene encodes a protein that contains a MIT 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 is a complicated type of hereditary spastic paraplegias . HSP is a category of neurological disorder characterized by spasticity and muscle weakness in the lower limbs.".
- SPG20 updateCitations "yes".
- SPG20 updatePage "yes".
- SPG20 updateProteinBox "yes".
- SPG20 updateSummary "yes".
- SPG20 wikiPageUsesTemplate Template:Gene-13-stub.
- SPG20 wikiPageUsesTemplate Template:PBB.
- SPG20 wikiPageUsesTemplate Template:PBB_Controls.
- SPG20 wikiPageUsesTemplate Template:PBB_Further_reading.
- SPG20 wikiPageUsesTemplate Template:PBB_Summary.
- SPG20 wikiPageUsesTemplate Template:PDB_Gallery.
- SPG20 wikiPageUsesTemplate Template:Refbegin.
- SPG20 wikiPageUsesTemplate Template:Refend.
- SPG20 wikiPageUsesTemplate Template:Reflist.
- SPG20 hypernym Protein.
- SPG20 type Biomolecule.
- SPG20 type Protein.
- SPG20 type Thing.
- SPG20 type Q206229.
- SPG20 type Q8054.
- SPG20 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).".
- SPG20 label "SPG20".
- SPG20 sameAs SPG20.
- SPG20 sameAs m.03g_slp.
- SPG20 sameAs Q7392539.
- SPG20 sameAs Q7392539.
- SPG20 wasDerivedFrom SPG20?oldid=679041118.
- SPG20 isPrimaryTopicOf SPG20.