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- Q2919537 subject Q6155998.
- Q2919537 subject Q9052781.
- Q2919537 abstract "Alglucosidase alfa (Lumizyme, Myozyme, Genzyme) is an enzyme replacement therapy (ERT) orphan drug for treatment of Pompe disease (Glycogen storage disease type II), a rare lysosomal storage disorder (LSD).Chemically speaking, the drug is an analog of the enzyme that is deficient in patients affected by Pompe disease, alpha-glucosidase. It is the first drug available to treat this disease.".
- Q2919537 atcPrefix "A16".
- Q2919537 atcSuffix "AB07".
- Q2919537 casNumber "420794-05-0".
- Q2919537 drugbank "DB01272".
- Q2919537 fdaUniiCode "DTI67O9503".
- Q2919537 iupacName "Human glucosidase, prepro-α-[199-arginine,223-histidine]".
- Q2919537 wikiPageExternalLink www.myozyme.com.
- Q2919537 wikiPageExternalLink mtap_pt.asp.
- Q2919537 wikiPageWikiLink Q12192.
- Q2919537 wikiPageWikiLink Q1365789.
- Q2919537 wikiPageWikiLink Q1367466.
- Q2919537 wikiPageWikiLink Q1502740.
- Q2919537 wikiPageWikiLink Q166231.
- Q2919537 wikiPageWikiLink Q181754.
- Q2919537 wikiPageWikiLink Q204711.
- Q2919537 wikiPageWikiLink Q2839456.
- Q2919537 wikiPageWikiLink Q38933.
- Q2919537 wikiPageWikiLink Q42982.
- Q2919537 wikiPageWikiLink Q485014.
- Q2919537 wikiPageWikiLink Q4917.
- Q2919537 wikiPageWikiLink Q6155998.
- Q2919537 wikiPageWikiLink Q675010.
- Q2919537 wikiPageWikiLink Q767485.
- Q2919537 wikiPageWikiLink Q9052781.
- Q2919537 wikiPageWikiLink Q916766.
- Q2919537 wikiPageWikiLink Q929833.
- Q2919537 atcPrefix "A16".
- Q2919537 atcSuffix "AB07".
- Q2919537 casNumber "420794".
- Q2919537 drugbank "DB01272".
- Q2919537 iupacName "Human glucosidase, prepro-α-[199-arginine,223-histidine]".
- Q2919537 unii "DTI67O9503".
- Q2919537 type ChemicalSubstance.
- Q2919537 type Drug.
- Q2919537 type ChemicalObject.
- Q2919537 type Thing.
- Q2919537 type Q8386.
- Q2919537 comment "Alglucosidase alfa (Lumizyme, Myozyme, Genzyme) is an enzyme replacement therapy (ERT) orphan drug for treatment of Pompe disease (Glycogen storage disease type II), a rare lysosomal storage disorder (LSD).Chemically speaking, the drug is an analog of the enzyme that is deficient in patients affected by Pompe disease, alpha-glucosidase. It is the first drug available to treat this disease.".
- Q2919537 label "Alglucosidase alfa".
- Q2919537 homepage www.myozyme.com.