Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Stargardt disease (STGD, also known as fundus flavimaculatus; FFM) is an autosomal recessive retinal disorder characterized by a juvenile-onset macular dystrophy, alterations of the peripheral retina, and subretinal deposition of lipofuscin-like material.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• assertion description "[Stargardt disease (STGD, also known as fundus flavimaculatus; FFM) is an autosomal recessive retinal disorder characterized by a juvenile-onset macular dystrophy, alterations of the peripheral retina, and subretinal deposition of lipofuscin-like material.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Stargardt disease (STGD, also known as fundus flavimaculatus; FFM) is an autosomal recessive retinal disorder characterized by a juvenile-onset macular dystrophy, alterations of the peripheral retina, and subretinal deposition of lipofuscin-like material.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Stargardt disease (STGD, also known as fundus flavimaculatus; FFM) is an autosomal recessive retinal disorder characterized by a juvenile-onset macular dystrophy, alterations of the peripheral retina, and subretinal deposition of lipofuscin-like material.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP681864.RADsmDSIskmxoIR3aXVNkBU8UwGBidkxs0pfhSddbjkzM130_assertion description "[Stargardt disease (STGD, also known as fundus flavimaculatus; FFM) is an autosomal recessive retinal disorder characterized by a juvenile-onset macular dystrophy, alterations of the peripheral retina, and subretinal deposition of lipofuscin-like material.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681864.RADsmDSIskmxoIR3aXVNkBU8UwGBidkxs0pfhSddbjkzM130_provenance.
• assertion description "[Stargardt disease (STGD, also known as fundus flavimaculatus; FFM) is an autosomal recessive retinal disorder characterized by a juvenile-onset macular dystrophy, alterations of the peripheral retina, and subretinal deposition of lipofuscin-like material.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP451234.RAfiAuMley5JRuBdvo6IJf0S0_wTNrQzNF32fjWIUnXsg130_assertion description "[Stargardt disease (STGD, also known as fundus flavimaculatus; FFM) is an autosomal recessive retinal disorder characterized by a juvenile-onset macular dystrophy, alterations of the peripheral retina, and subretinal deposition of lipofuscin-like material.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP451234.RAfiAuMley5JRuBdvo6IJf0S0_wTNrQzNF32fjWIUnXsg130_provenance.
• NP1368516.RAQbwvmuSzzcfYOOr2iaz0pXF7i5Je14bHFh8B7COKo9w130_assertion description "[Stargardt disease (STGD, also known as fundus flavimaculatus; FFM) is an autosomal recessive retinal disorder characterized by a juvenile-onset macular dystrophy, alterations of the peripheral retina, and subretinal deposition of lipofuscin-like material.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1368516.RAQbwvmuSzzcfYOOr2iaz0pXF7i5Je14bHFh8B7COKo9w130_provenance.
• NP1368518.RAYzavcmoXc9ShDg8Q3--Ys3gMwcX8c_j92g8tOTfQBws130_assertion description "[Stargardt disease (STGD, also known as fundus flavimaculatus; FFM) is an autosomal recessive retinal disorder characterized by a juvenile-onset macular dystrophy, alterations of the peripheral retina, and subretinal deposition of lipofuscin-like material.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1368518.RAYzavcmoXc9ShDg8Q3--Ys3gMwcX8c_j92g8tOTfQBws130_provenance.
• NP1368519.RAXn0Rsa4SwlGSxZcu5IK82ss9qUueqeJ86G4IAvU_Q4M130_assertion description "[Stargardt disease (STGD, also known as fundus flavimaculatus; FFM) is an autosomal recessive retinal disorder characterized by a juvenile-onset macular dystrophy, alterations of the peripheral retina, and subretinal deposition of lipofuscin-like material.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1368519.RAXn0Rsa4SwlGSxZcu5IK82ss9qUueqeJ86G4IAvU_Q4M130_provenance.
• NP1368517.RAGciPrgvihZ_gao-RbKe1h7SWagTG7tucdU12TbkfpJw130_assertion description "[Stargardt disease (STGD, also known as fundus flavimaculatus; FFM) is an autosomal recessive retinal disorder characterized by a juvenile-onset macular dystrophy, alterations of the peripheral retina, and subretinal deposition of lipofuscin-like material.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1368517.RAGciPrgvihZ_gao-RbKe1h7SWagTG7tucdU12TbkfpJw130_provenance.