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- Aspartylglucosaminidase abstract "N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase is an enzyme that in humans is encoded by the AGA gene.Aspartylglucosaminidase is an amidohydrolase enzyme involved in the catabolism of N-linked oligosaccharides of glycoproteins. It cleaves asparagine from N-acetylglucosamines as one of the final steps in the lysosomal breakdown of glycoproteins. The lysosomal storage disease aspartylglycosaminuria is caused by a deficiency in the AGA enzyme.".
- Aspartylglucosaminidase entrezgene "175".
- Aspartylglucosaminidase wikiPageID "6702076".
- Aspartylglucosaminidase wikiPageLength "6992".
- Aspartylglucosaminidase wikiPageOutDegree "7".
- Aspartylglucosaminidase wikiPageRevisionID "659797943".
- Aspartylglucosaminidase wikiPageWikiLink Amidohydrolase.
- Aspartylglucosaminidase wikiPageWikiLink Aspartylglucosaminuria.
- Aspartylglucosaminidase wikiPageWikiLink Enzyme.
- Aspartylglucosaminidase wikiPageWikiLink Gene.
- Aspartylglucosaminidase wikiPageWikiLink Glycoprotein.
- Aspartylglucosaminidase wikiPageWikiLink N-linked_oligosaccharides.
- Aspartylglucosaminidase wikiPageWikiLinkText "AGA".
- Aspartylglucosaminidase wikiPageWikiLinkText "Aspartylglucosaminidase".
- Aspartylglucosaminidase wikiPageWikiLinkText "aspartylglucosaminidase".
- Aspartylglucosaminidase requireManualInspection "no".
- Aspartylglucosaminidase summaryText "Aspartylglucosaminidase is an amidohydrolase enzyme involved in the catabolism of N-linked oligosaccharides of glycoproteins. It cleaves asparagine from N-acetylglucosamines as one of the final steps in the lysosomal breakdown of glycoproteins. The lysosomal storage disease aspartylglycosaminuria is caused by a deficiency in the AGA enzyme.".
- Aspartylglucosaminidase updateCitations "yes".
- Aspartylglucosaminidase updatePage "yes".
- Aspartylglucosaminidase updateProteinBox "yes".
- Aspartylglucosaminidase updateSummary "no".
- Aspartylglucosaminidase wikiPageUsesTemplate Template:Carbon-nitrogen_non-peptide_hydrolases.
- Aspartylglucosaminidase wikiPageUsesTemplate Template:Cite_journal.
- Aspartylglucosaminidase wikiPageUsesTemplate Template:Glycoprotein_catabolism.
- Aspartylglucosaminidase wikiPageUsesTemplate Template:Hydrolase-stub.
- Aspartylglucosaminidase wikiPageUsesTemplate Template:MeshName.
- Aspartylglucosaminidase wikiPageUsesTemplate Template:PBB.
- Aspartylglucosaminidase wikiPageUsesTemplate Template:PBB_Controls.
- Aspartylglucosaminidase wikiPageUsesTemplate Template:PBB_Further_reading.
- Aspartylglucosaminidase wikiPageUsesTemplate Template:PBB_Summary.
- Aspartylglucosaminidase wikiPageUsesTemplate Template:PDB_Gallery.
- Aspartylglucosaminidase wikiPageUsesTemplate Template:Refbegin.
- Aspartylglucosaminidase wikiPageUsesTemplate Template:Refend.
- Aspartylglucosaminidase wikiPageUsesTemplate Template:Reflist.
- Aspartylglucosaminidase hypernym Enzyme.
- Aspartylglucosaminidase type Biomolecule.
- Aspartylglucosaminidase type Protein.
- Aspartylglucosaminidase type Thing.
- Aspartylglucosaminidase type Q206229.
- Aspartylglucosaminidase type Q8054.
- Aspartylglucosaminidase comment "N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase is an enzyme that in humans is encoded by the AGA gene.Aspartylglucosaminidase is an amidohydrolase enzyme involved in the catabolism of N-linked oligosaccharides of glycoproteins. It cleaves asparagine from N-acetylglucosamines as one of the final steps in the lysosomal breakdown of glycoproteins. The lysosomal storage disease aspartylglycosaminuria is caused by a deficiency in the AGA enzyme.".
- Aspartylglucosaminidase label "Aspartylglucosaminidase".
- Aspartylglucosaminidase sameAs Q18247637.
- Aspartylglucosaminidase sameAs m.0gj2ds.
- Aspartylglucosaminidase sameAs Q18247637.
- Aspartylglucosaminidase wasDerivedFrom Aspartylglucosaminidase?oldid=659797943.
- Aspartylglucosaminidase isPrimaryTopicOf Aspartylglucosaminidase.