Matches in Nanopublications for { ?s ?p "[Galactosialidosis is a recessively inherited lysosomal storage disease characterized by the combined deficiency of neuraminidase and beta-galactosidase secondary to the genetic deficiency of cathepsin A/protective protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP273993.RATea17F_mTwAiggRABBX3TyAuyQ2jwJHaRPehDozCzLc130_assertion description "[Galactosialidosis is a recessively inherited lysosomal storage disease characterized by the combined deficiency of neuraminidase and beta-galactosidase secondary to the genetic deficiency of cathepsin A/protective protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP273993.RATea17F_mTwAiggRABBX3TyAuyQ2jwJHaRPehDozCzLc130_provenance.
- NP616322.RATzk9TbIESTSZe_TaC5FlkrHuSyL60piJFOMvVk4aQYE130_assertion description "[Galactosialidosis is a recessively inherited lysosomal storage disease characterized by the combined deficiency of neuraminidase and beta-galactosidase secondary to the genetic deficiency of cathepsin A/protective protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616322.RATzk9TbIESTSZe_TaC5FlkrHuSyL60piJFOMvVk4aQYE130_provenance.
- assertion description "[Galactosialidosis is a recessively inherited lysosomal storage disease characterized by the combined deficiency of neuraminidase and beta-galactosidase secondary to the genetic deficiency of cathepsin A/protective protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Galactosialidosis is a recessively inherited lysosomal storage disease characterized by the combined deficiency of neuraminidase and beta-galactosidase secondary to the genetic deficiency of cathepsin A/protective protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Galactosialidosis is a recessively inherited lysosomal storage disease characterized by the combined deficiency of neuraminidase and beta-galactosidase secondary to the genetic deficiency of cathepsin A/protective protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP802496.RAkzsH7shBSOD5bAMzptYJCpBSk8TfcNdCj8BrmL8oCGI130_assertion description "[Galactosialidosis is a recessively inherited lysosomal storage disease characterized by the combined deficiency of neuraminidase and beta-galactosidase secondary to the genetic deficiency of cathepsin A/protective protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802496.RAkzsH7shBSOD5bAMzptYJCpBSk8TfcNdCj8BrmL8oCGI130_provenance.
- NP427412.RAbcEsIv-VWmrUteGssVHoWHu6kURspY9imDXrwGNdiMY130_assertion description "[Galactosialidosis is a recessively inherited lysosomal storage disease characterized by the combined deficiency of neuraminidase and beta-galactosidase secondary to the genetic deficiency of cathepsin A/protective protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP427412.RAbcEsIv-VWmrUteGssVHoWHu6kURspY9imDXrwGNdiMY130_provenance.
- NP427420.RAXNh88MPI60lx4qDlGg2wrIUBPNDWZ82xNwMqoOT-wsk130_assertion description "[Galactosialidosis is a recessively inherited lysosomal storage disease characterized by the combined deficiency of neuraminidase and beta-galactosidase secondary to the genetic deficiency of cathepsin A/protective protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP427420.RAXNh88MPI60lx4qDlGg2wrIUBPNDWZ82xNwMqoOT-wsk130_provenance.
- NP860819.RAKShtkDZL7VLbKpe_zpUTVbJ2O16WLRHzlvgb-8UoOdY130_assertion description "[Galactosialidosis is a recessively inherited lysosomal storage disease characterized by the combined deficiency of neuraminidase and beta-galactosidase secondary to the genetic deficiency of cathepsin A/protective protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP860819.RAKShtkDZL7VLbKpe_zpUTVbJ2O16WLRHzlvgb-8UoOdY130_provenance.
- NP1395990.RArbqCrgYE7TgxcFLDccy9JJ0ONi7HV7goqsHvSXETo9g130_assertion description "[Galactosialidosis is a recessively inherited lysosomal storage disease characterized by the combined deficiency of neuraminidase and beta-galactosidase secondary to the genetic deficiency of cathepsin A/protective protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1395990.RArbqCrgYE7TgxcFLDccy9JJ0ONi7HV7goqsHvSXETo9g130_provenance.
- NP1395992.RAmX8yOwoHNA5q6ss0zDlhFj0RxzY0eIGE5y1n4H0vrtE130_assertion description "[Galactosialidosis is a recessively inherited lysosomal storage disease characterized by the combined deficiency of neuraminidase and beta-galactosidase secondary to the genetic deficiency of cathepsin A/protective protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1395992.RAmX8yOwoHNA5q6ss0zDlhFj0RxzY0eIGE5y1n4H0vrtE130_provenance.
- NP427324.RA-8e5KGuPf1eYPqoctrNTibZNLTR6MJhy6z2nXcS0NvQ130_assertion description "[Galactosialidosis is a recessively inherited lysosomal storage disease characterized by the combined deficiency of neuraminidase and beta-galactosidase secondary to the genetic deficiency of cathepsin A/protective protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP427324.RA-8e5KGuPf1eYPqoctrNTibZNLTR6MJhy6z2nXcS0NvQ130_provenance.
- NP1395991.RA4JQAiqPTVx8lT_NGfKtWlGXntpsm6SJpMMaLfxGZptQ130_assertion description "[Galactosialidosis is a recessively inherited lysosomal storage disease characterized by the combined deficiency of neuraminidase and beta-galactosidase secondary to the genetic deficiency of cathepsin A/protective protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1395991.RA4JQAiqPTVx8lT_NGfKtWlGXntpsm6SJpMMaLfxGZptQ130_provenance.