Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[The human lysosomal enzyme occurs in complex with beta-galactosidase and protective protein/cathepsin A (PPCA), and is deficient in two genetic disorders: sialidosis, caused by a structural defect in the neuraminidase gene, and galactosialidosis, in which the loss of neuraminidase activity is secondary to a deficiency of PPCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP673232.RAlBFvuvVhwA4P64GRsW0Imv8lmDBHh2itr35acVQ5ZPk130_assertion description "[The human lysosomal enzyme occurs in complex with beta-galactosidase and protective protein/cathepsin A (PPCA), and is deficient in two genetic disorders: sialidosis, caused by a structural defect in the neuraminidase gene, and galactosialidosis, in which the loss of neuraminidase activity is secondary to a deficiency of PPCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP673232.RAlBFvuvVhwA4P64GRsW0Imv8lmDBHh2itr35acVQ5ZPk130_provenance.
• NP780470.RAq-gIrZFaaO-DoVUobruBebyF8H2w4p3F8jU2hOijNUY130_assertion description "[The human lysosomal enzyme occurs in complex with beta-galactosidase and protective protein/cathepsin A (PPCA), and is deficient in two genetic disorders: sialidosis, caused by a structural defect in the neuraminidase gene, and galactosialidosis, in which the loss of neuraminidase activity is secondary to a deficiency of PPCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP780470.RAq-gIrZFaaO-DoVUobruBebyF8H2w4p3F8jU2hOijNUY130_provenance.
• NP469140.RAxxjsJdOI2lsumW_cW_W31rWMgBq_6NwWcVEg5OOZ9ek130_assertion description "[The human lysosomal enzyme occurs in complex with beta-galactosidase and protective protein/cathepsin A (PPCA), and is deficient in two genetic disorders: sialidosis, caused by a structural defect in the neuraminidase gene, and galactosialidosis, in which the loss of neuraminidase activity is secondary to a deficiency of PPCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP469140.RAxxjsJdOI2lsumW_cW_W31rWMgBq_6NwWcVEg5OOZ9ek130_provenance.
• NP620659.RA_6qZWQhnCPk07-OQe-hMDzhyWjfo5Z8dmRSeXuwj3fU130_assertion description "[The human lysosomal enzyme occurs in complex with beta-galactosidase and protective protein/cathepsin A (PPCA), and is deficient in two genetic disorders: sialidosis, caused by a structural defect in the neuraminidase gene, and galactosialidosis, in which the loss of neuraminidase activity is secondary to a deficiency of PPCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP620659.RA_6qZWQhnCPk07-OQe-hMDzhyWjfo5Z8dmRSeXuwj3fU130_provenance.
• NP505711.RA5O3Yf80Br12fSPnsw_ZTj1GnN6DgR2fOOu9BPmX6SK8130_assertion description "[The human lysosomal enzyme occurs in complex with beta-galactosidase and protective protein/cathepsin A (PPCA), and is deficient in two genetic disorders: sialidosis, caused by a structural defect in the neuraminidase gene, and galactosialidosis, in which the loss of neuraminidase activity is secondary to a deficiency of PPCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP505711.RA5O3Yf80Br12fSPnsw_ZTj1GnN6DgR2fOOu9BPmX6SK8130_provenance.
• assertion description "[The human lysosomal enzyme occurs in complex with beta-galactosidase and protective protein/cathepsin A (PPCA), and is deficient in two genetic disorders: sialidosis, caused by a structural defect in the neuraminidase gene, and galactosialidosis, in which the loss of neuraminidase activity is secondary to a deficiency of PPCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP638241.RAD4nDfwJ7aUBsAoEoJKZG8Ahr-5mtF8K6BVkgD-qozUk130_assertion description "[The human lysosomal enzyme occurs in complex with beta-galactosidase and protective protein/cathepsin A (PPCA), and is deficient in two genetic disorders: sialidosis, caused by a structural defect in the neuraminidase gene, and galactosialidosis, in which the loss of neuraminidase activity is secondary to a deficiency of PPCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP638241.RAD4nDfwJ7aUBsAoEoJKZG8Ahr-5mtF8K6BVkgD-qozUk130_provenance.
• NP427170.RAiEJazCT28gUE4Yt-y1FOP1dbnKboevi8s4TXe2jGDew130_assertion description "[The human lysosomal enzyme occurs in complex with beta-galactosidase and protective protein/cathepsin A (PPCA), and is deficient in two genetic disorders: sialidosis, caused by a structural defect in the neuraminidase gene, and galactosialidosis, in which the loss of neuraminidase activity is secondary to a deficiency of PPCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP427170.RAiEJazCT28gUE4Yt-y1FOP1dbnKboevi8s4TXe2jGDew130_provenance.
• NP1365133.RADHhq7cGUq8aqquARgSA7Ar06Gay_HkD08jsN36KPymg130_assertion description "[The human lysosomal enzyme occurs in complex with beta-galactosidase and protective protein/cathepsin A (PPCA), and is deficient in two genetic disorders: sialidosis, caused by a structural defect in the neuraminidase gene, and galactosialidosis, in which the loss of neuraminidase activity is secondary to a deficiency of PPCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1365133.RADHhq7cGUq8aqquARgSA7Ar06Gay_HkD08jsN36KPymg130_provenance.
• NP427419.RA32m96afu9-FvqM37P8b7cQSAw_XkrbV-N9sr5Hkght4130_assertion description "[The human lysosomal enzyme occurs in complex with beta-galactosidase and protective protein/cathepsin A (PPCA), and is deficient in two genetic disorders: sialidosis, caused by a structural defect in the neuraminidase gene, and galactosialidosis, in which the loss of neuraminidase activity is secondary to a deficiency of PPCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP427419.RA32m96afu9-FvqM37P8b7cQSAw_XkrbV-N9sr5Hkght4130_provenance.
• NP1365132.RA2uicdBdYcZ5vBmLr9R_wGkxz59c2JY89IIDFhaQNxvo130_assertion description "[The human lysosomal enzyme occurs in complex with beta-galactosidase and protective protein/cathepsin A (PPCA), and is deficient in two genetic disorders: sialidosis, caused by a structural defect in the neuraminidase gene, and galactosialidosis, in which the loss of neuraminidase activity is secondary to a deficiency of PPCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1365132.RA2uicdBdYcZ5vBmLr9R_wGkxz59c2JY89IIDFhaQNxvo130_provenance.