Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Loss-of-function mutations in the gene (CSTB) encoding human cystatin B, a widely expressed cysteine protease inhibitor, are responsible for a severe neurological disorder known as Unverricht-Lundborg disease (EPM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• assertion description "[Loss-of-function mutations in the gene (CSTB) encoding human cystatin B, a widely expressed cysteine protease inhibitor, are responsible for a severe neurological disorder known as Unverricht-Lundborg disease (EPM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Loss-of-function mutations in the gene (CSTB) encoding human cystatin B, a widely expressed cysteine protease inhibitor, are responsible for a severe neurological disorder known as Unverricht-Lundborg disease (EPM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Loss-of-function mutations in the gene (CSTB) encoding human cystatin B, a widely expressed cysteine protease inhibitor, are responsible for a severe neurological disorder known as Unverricht-Lundborg disease (EPM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP333874.RAexRgKa7xpjZPK6lmoIFWhM5pOVPL1-QHHYmHvZtBihA130_assertion description "[Loss-of-function mutations in the gene (CSTB) encoding human cystatin B, a widely expressed cysteine protease inhibitor, are responsible for a severe neurological disorder known as Unverricht-Lundborg disease (EPM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333874.RAexRgKa7xpjZPK6lmoIFWhM5pOVPL1-QHHYmHvZtBihA130_provenance.
• NP337103.RAf9PTF4uK4XqygxCv_WGlbMO4Cz6b66dPFOvtFQpQCoA130_assertion description "[Loss-of-function mutations in the gene (CSTB) encoding human cystatin B, a widely expressed cysteine protease inhibitor, are responsible for a severe neurological disorder known as Unverricht-Lundborg disease (EPM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP337103.RAf9PTF4uK4XqygxCv_WGlbMO4Cz6b66dPFOvtFQpQCoA130_provenance.
• NP828924.RA_Wa6Iye9S0B7Hp6BkxqY_aSnFMSbdRvdI9HROPmd3XY130_assertion description "[Loss-of-function mutations in the gene (CSTB) encoding human cystatin B, a widely expressed cysteine protease inhibitor, are responsible for a severe neurological disorder known as Unverricht-Lundborg disease (EPM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP828924.RA_Wa6Iye9S0B7Hp6BkxqY_aSnFMSbdRvdI9HROPmd3XY130_provenance.
• NP989681.RAaF2JtrPZbySfkH9pjLdESv-Y2IYML1McTRlT0e18YIo130_assertion description "[Loss-of-function mutations in the gene (CSTB) encoding human cystatin B, a widely expressed cysteine protease inhibitor, are responsible for a severe neurological disorder known as Unverricht-Lundborg disease (EPM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP989681.RAaF2JtrPZbySfkH9pjLdESv-Y2IYML1McTRlT0e18YIo130_provenance.
• assertion description "[Loss-of-function mutations in the gene (CSTB) encoding human cystatin B, a widely expressed cysteine protease inhibitor, are responsible for a severe neurological disorder known as Unverricht-Lundborg disease (EPM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Loss-of-function mutations in the gene (CSTB) encoding human cystatin B, a widely expressed cysteine protease inhibitor, are responsible for a severe neurological disorder known as Unverricht-Lundborg disease (EPM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP1407574.RAi5ysf8sYp0tAF2NRMu8KTzIvYKvUdi_YvJsczgmub34130_assertion description "[Loss-of-function mutations in the gene (CSTB) encoding human cystatin B, a widely expressed cysteine protease inhibitor, are responsible for a severe neurological disorder known as Unverricht-Lundborg disease (EPM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1407574.RAi5ysf8sYp0tAF2NRMu8KTzIvYKvUdi_YvJsczgmub34130_provenance.
• NP1407576.RAoFcz4KQVbNSjC9Ighu0O0YAC-EUYucCjZMEkoSsAVeA130_assertion description "[Loss-of-function mutations in the gene (CSTB) encoding human cystatin B, a widely expressed cysteine protease inhibitor, are responsible for a severe neurological disorder known as Unverricht-Lundborg disease (EPM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1407576.RAoFcz4KQVbNSjC9Ighu0O0YAC-EUYucCjZMEkoSsAVeA130_provenance.
• NP1407573.RAAYds-zPp5KXCKYnTt0HV4sxa1tjY0tfMuXPmQmMiDf8130_assertion description "[Loss-of-function mutations in the gene (CSTB) encoding human cystatin B, a widely expressed cysteine protease inhibitor, are responsible for a severe neurological disorder known as Unverricht-Lundborg disease (EPM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1407573.RAAYds-zPp5KXCKYnTt0HV4sxa1tjY0tfMuXPmQmMiDf8130_provenance.
• NP337244.RA2w6KLXlMtWbcLefbqtS-E-3BfggLZZjtSRz98skEUQs130_assertion description "[Loss-of-function mutations in the gene (CSTB) encoding human cystatin B, a widely expressed cysteine protease inhibitor, are responsible for a severe neurological disorder known as Unverricht-Lundborg disease (EPM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP337244.RA2w6KLXlMtWbcLefbqtS-E-3BfggLZZjtSRz98skEUQs130_provenance.
• NP989823.RAHMw7PupmO-MBUnXt-sKVzhkZsg5yuMHB1yxCk4SYitU130_assertion description "[Loss-of-function mutations in the gene (CSTB) encoding human cystatin B, a widely expressed cysteine protease inhibitor, are responsible for a severe neurological disorder known as Unverricht-Lundborg disease (EPM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP989823.RAHMw7PupmO-MBUnXt-sKVzhkZsg5yuMHB1yxCk4SYitU130_provenance.
• NP1407571.RAJ4XSP9MHXJSPB9Hc2pMNwfatu8662xeDMiXTSZ_Q1qk130_assertion description "[Loss-of-function mutations in the gene (CSTB) encoding human cystatin B, a widely expressed cysteine protease inhibitor, are responsible for a severe neurological disorder known as Unverricht-Lundborg disease (EPM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1407571.RAJ4XSP9MHXJSPB9Hc2pMNwfatu8662xeDMiXTSZ_Q1qk130_provenance.
• NP1407572.RAMzuPH_xqo8UDgggFiyclDBBBDkBd7yf2EMEzR0L3EXk130_assertion description "[Loss-of-function mutations in the gene (CSTB) encoding human cystatin B, a widely expressed cysteine protease inhibitor, are responsible for a severe neurological disorder known as Unverricht-Lundborg disease (EPM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1407572.RAMzuPH_xqo8UDgggFiyclDBBBDkBd7yf2EMEzR0L3EXk130_provenance.