Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP655388.RAY3tYvLu9YA2u0xZDSBpvkOyzVntl1gqrJoI15HHvVzk130_assertion description "[Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP655388.RAY3tYvLu9YA2u0xZDSBpvkOyzVntl1gqrJoI15HHvVzk130_provenance.
• NP6120.RAoQw2tuSCu-CF5M_mIjW9HIQPc89sLjFA-1brabzjvGw130_assertion description "[Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6120.RAoQw2tuSCu-CF5M_mIjW9HIQPc89sLjFA-1brabzjvGw130_provenance.
• assertion description "[Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP6914.RAXR9Z-17bAqS2DlZet_qVIt8Lacj9Pi-Cg7GgyJ9j0d8130_assertion description "[Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6914.RAXR9Z-17bAqS2DlZet_qVIt8Lacj9Pi-Cg7GgyJ9j0d8130_provenance.
• NP30651.RAa5zztAOrw5GPHGYeTjtRB9O6gVfRmflVyYhDVDxqXN0130_assertion description "[Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30651.RAa5zztAOrw5GPHGYeTjtRB9O6gVfRmflVyYhDVDxqXN0130_provenance.
• assertion description "[Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP30646.RAujmt4TTgbK-4g8KT2Am_-p1y6T2MgSInnADc0E6pO1Q130_assertion description "[Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30646.RAujmt4TTgbK-4g8KT2Am_-p1y6T2MgSInnADc0E6pO1Q130_provenance.
• NP30650.RAhHq97b6LOxZHOr1A3HrTAXb5OZn06ohfXDZJwkuoYUQ130_assertion description "[Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30650.RAhHq97b6LOxZHOr1A3HrTAXb5OZn06ohfXDZJwkuoYUQ130_provenance.
• NP30647.RAG-hMI8qa58M_EG9y7HTM5UKvPP0STUkIKyr6q8l9pKg130_assertion description "[Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30647.RAG-hMI8qa58M_EG9y7HTM5UKvPP0STUkIKyr6q8l9pKg130_provenance.
• NP30648.RAKNnpv8tNYNowAWNf9eP17T0Lx_MzAPdR6yyX9z-7rbE130_assertion description "[Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30648.RAKNnpv8tNYNowAWNf9eP17T0Lx_MzAPdR6yyX9z-7rbE130_provenance.
• NP30649.RA1XyxpDWZFOyPjUB8PZOVdHfpAV97nPnEWs7mqvX0OVo130_assertion description "[Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30649.RA1XyxpDWZFOyPjUB8PZOVdHfpAV97nPnEWs7mqvX0OVo130_provenance.