Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP755853.RAdp267jaYnkAPi7tdtlClctD1hLZ1OSRuYEs-u5E7_v8130_assertion description "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755853.RAdp267jaYnkAPi7tdtlClctD1hLZ1OSRuYEs-u5E7_v8130_provenance.
• assertion description "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP714427.RAx96TpJAIKbNQW_t_hOLg72WYKt4f64AIokuHX8JwoGY130_assertion description "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP714427.RAx96TpJAIKbNQW_t_hOLg72WYKt4f64AIokuHX8JwoGY130_provenance.
• NP653713.RA5uQjZB0OgvlM4ZqgMjkUM_xFCMJcT2BaIQe7BK8YXb8130_assertion description "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP653713.RA5uQjZB0OgvlM4ZqgMjkUM_xFCMJcT2BaIQe7BK8YXb8130_provenance.
• NP268761.RAAo7YNfq1MMOd5_CGRrd7CW0z7GzOJ9qZ64HxwvI5Wg4130_assertion description "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP268761.RAAo7YNfq1MMOd5_CGRrd7CW0z7GzOJ9qZ64HxwvI5Wg4130_provenance.
• NP328056.RAjevLk7gEnFz-BMoYUB9QwrtgOstVrX3dZB8jQFevMK8130_assertion description "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP328056.RAjevLk7gEnFz-BMoYUB9QwrtgOstVrX3dZB8jQFevMK8130_provenance.
• NP328100.RAkcuN9FA1Aa9R3ECssUrsAH9ofo5f12KA1K9WoI9YODE130_assertion description "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP328100.RAkcuN9FA1Aa9R3ECssUrsAH9ofo5f12KA1K9WoI9YODE130_provenance.
• NP268760.RAQenNBj-qSq4zN2SwxzKt9QUalV7NIr76l3sIdnfw6nE130_assertion description "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP268760.RAQenNBj-qSq4zN2SwxzKt9QUalV7NIr76l3sIdnfw6nE130_provenance.
• NP268762.RAZKJMlN7wsdFLjNEQzrAbZkD2fHmLRiXupyBlgTum_9w130_assertion description "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP268762.RAZKJMlN7wsdFLjNEQzrAbZkD2fHmLRiXupyBlgTum_9w130_provenance.
• NP268763.RAgQX3ejLZ6OR5lrhH3p5pe3h1Ar9_yHTNrtX66BIUOQk130_assertion description "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP268763.RAgQX3ejLZ6OR5lrhH3p5pe3h1Ar9_yHTNrtX66BIUOQk130_provenance.
• NP889876.RAHMAngPJKDIBkSCCbyzcoUKuNyP0uiuu3fZvmEVaCNYA130_assertion description "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889876.RAHMAngPJKDIBkSCCbyzcoUKuNyP0uiuu3fZvmEVaCNYA130_provenance.
• NP328101.RA_6FS-CRk2TBuKkqG0izSJeg_XYIP6HXshrMTxJHK92U130_assertion description "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP328101.RA_6FS-CRk2TBuKkqG0izSJeg_XYIP6HXshrMTxJHK92U130_provenance.
• NP268759.RAyxfXn7qHbkj-dMrJP6TvEZZiPBGCWO-Pg3XjVUNp7lU130_assertion description "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP268759.RAyxfXn7qHbkj-dMrJP6TvEZZiPBGCWO-Pg3XjVUNp7lU130_provenance.