Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Inactivating mutations in the retinoid isomerase (RPE65) or lecithin:retinol acyltransferase (LRAT) genes cause Leber congenital amaurosis (LCA), a severe visual impairment in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP906355.RAWfts2D3nFxQ_yuaG6QJqgUZUHhpDRrqAMKB15mX44lg130_assertion description "[Inactivating mutations in the retinoid isomerase (RPE65) or lecithin:retinol acyltransferase (LRAT) genes cause Leber congenital amaurosis (LCA), a severe visual impairment in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP906355.RAWfts2D3nFxQ_yuaG6QJqgUZUHhpDRrqAMKB15mX44lg130_provenance.
• NP21823.RAoI_qU_fD886a0c9I3m_ExUeANziFrLXbRePdVmWapIo130_assertion description "[Inactivating mutations in the retinoid isomerase (RPE65) or lecithin:retinol acyltransferase (LRAT) genes cause Leber congenital amaurosis (LCA), a severe visual impairment in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP21823.RAoI_qU_fD886a0c9I3m_ExUeANziFrLXbRePdVmWapIo130_provenance.
• NP564134.RAj-tzV5C-c_sELSWAMLZj7RrDUFrInmAbSJlHiSgNkRQ130_assertion description "[Inactivating mutations in the retinoid isomerase (RPE65) or lecithin:retinol acyltransferase (LRAT) genes cause Leber congenital amaurosis (LCA), a severe visual impairment in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP564134.RAj-tzV5C-c_sELSWAMLZj7RrDUFrInmAbSJlHiSgNkRQ130_provenance.
• NP401551.RAReQNdFTmvo1HTSnF92USiqV5DVfQUDjOZKjgZk74TxI130_assertion description "[Inactivating mutations in the retinoid isomerase (RPE65) or lecithin:retinol acyltransferase (LRAT) genes cause Leber congenital amaurosis (LCA), a severe visual impairment in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401551.RAReQNdFTmvo1HTSnF92USiqV5DVfQUDjOZKjgZk74TxI130_provenance.
• NP818242.RABGvEz20krkzDidZc961DBSIkGt966jk2qLYMqcRupWk130_assertion description "[Inactivating mutations in the retinoid isomerase (RPE65) or lecithin:retinol acyltransferase (LRAT) genes cause Leber congenital amaurosis (LCA), a severe visual impairment in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP818242.RABGvEz20krkzDidZc961DBSIkGt966jk2qLYMqcRupWk130_provenance.
• NP21225.RA_cw6n88eHeR_40vDmtNd5FW9X9xS0hUq3bykfsIfMsk130_assertion description "[Inactivating mutations in the retinoid isomerase (RPE65) or lecithin:retinol acyltransferase (LRAT) genes cause Leber congenital amaurosis (LCA), a severe visual impairment in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP21225.RA_cw6n88eHeR_40vDmtNd5FW9X9xS0hUq3bykfsIfMsk130_provenance.
• NP674980.RAcNGN1d7w_xkgxM8XI2OlHDnle7L5nmbEQrEecvuOpAc130_assertion description "[Inactivating mutations in the retinoid isomerase (RPE65) or lecithin:retinol acyltransferase (LRAT) genes cause Leber congenital amaurosis (LCA), a severe visual impairment in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674980.RAcNGN1d7w_xkgxM8XI2OlHDnle7L5nmbEQrEecvuOpAc130_provenance.
• NP729975.RA_wCxaC48UHZS71l6hIk8h0S-IzQw1OlBsaa-7ZgJ-KE130_assertion description "[Inactivating mutations in the retinoid isomerase (RPE65) or lecithin:retinol acyltransferase (LRAT) genes cause Leber congenital amaurosis (LCA), a severe visual impairment in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP729975.RA_wCxaC48UHZS71l6hIk8h0S-IzQw1OlBsaa-7ZgJ-KE130_provenance.
• NP729973.RAfxcBVvOhLpiSbK80KQizsXHt4gv_gmy3YlQtEsyLmKc130_assertion description "[Inactivating mutations in the retinoid isomerase (RPE65) or lecithin:retinol acyltransferase (LRAT) genes cause Leber congenital amaurosis (LCA), a severe visual impairment in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP729973.RAfxcBVvOhLpiSbK80KQizsXHt4gv_gmy3YlQtEsyLmKc130_provenance.
• NP729974.RAXUEfCiPYxnZDdAd9FPLpPp5HqclC5JMg6uSa14Ca6Ds130_assertion description "[Inactivating mutations in the retinoid isomerase (RPE65) or lecithin:retinol acyltransferase (LRAT) genes cause Leber congenital amaurosis (LCA), a severe visual impairment in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP729974.RAXUEfCiPYxnZDdAd9FPLpPp5HqclC5JMg6uSa14Ca6Ds130_provenance.
• NP729976.RAXPJ4bpfflPJW3v19d6MyyHtvUzRRBu_V9ZTVA0yo3vg130_assertion description "[Inactivating mutations in the retinoid isomerase (RPE65) or lecithin:retinol acyltransferase (LRAT) genes cause Leber congenital amaurosis (LCA), a severe visual impairment in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP729976.RAXPJ4bpfflPJW3v19d6MyyHtvUzRRBu_V9ZTVA0yo3vg130_provenance.
• assertion description "[Inactivating mutations in the retinoid isomerase (RPE65) or lecithin:retinol acyltransferase (LRAT) genes cause Leber congenital amaurosis (LCA), a severe visual impairment in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Inactivating mutations in the retinoid isomerase (RPE65) or lecithin:retinol acyltransferase (LRAT) genes cause Leber congenital amaurosis (LCA), a severe visual impairment in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Inactivating mutations in the retinoid isomerase (RPE65) or lecithin:retinol acyltransferase (LRAT) genes cause Leber congenital amaurosis (LCA), a severe visual impairment in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Inactivating mutations in the retinoid isomerase (RPE65) or lecithin:retinol acyltransferase (LRAT) genes cause Leber congenital amaurosis (LCA), a severe visual impairment in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Inactivating mutations in the retinoid isomerase (RPE65) or lecithin:retinol acyltransferase (LRAT) genes cause Leber congenital amaurosis (LCA), a severe visual impairment in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Inactivating mutations in the retinoid isomerase (RPE65) or lecithin:retinol acyltransferase (LRAT) genes cause Leber congenital amaurosis (LCA), a severe visual impairment in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Inactivating mutations in the retinoid isomerase (RPE65) or lecithin:retinol acyltransferase (LRAT) genes cause Leber congenital amaurosis (LCA), a severe visual impairment in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP818232.RAvPvlzu5Auwk27phXDEaMXDK9zZsNtYg3rVubxyDS2Eo130_assertion description "[Inactivating mutations in the retinoid isomerase (RPE65) or lecithin:retinol acyltransferase (LRAT) genes cause Leber congenital amaurosis (LCA), a severe visual impairment in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP818232.RAvPvlzu5Auwk27phXDEaMXDK9zZsNtYg3rVubxyDS2Eo130_provenance.