Matches in Nanopublications for { ?s ?p "[For example, mutations in the ABCR gene, (recently identified in cones as well) which codes for retinal rod-specific ABCR protein is responsible for Stargardt macular dystrophy/fundus flavimaculatus, an autosomal recessive macular dystrophy with juvenile onset, which accounts for 7% of human retinal degenerative diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[For example, mutations in the ABCR gene, (recently identified in cones as well) which codes for retinal rod-specific ABCR protein is responsible for Stargardt macular dystrophy/fundus flavimaculatus, an autosomal recessive macular dystrophy with juvenile onset, which accounts for 7% of human retinal degenerative diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP610669.RAsmSYYJ6K9apNbbxsUCbitkygBBsrsVM9xX_I9Tc9Ybo130_assertion description "[For example, mutations in the ABCR gene, (recently identified in cones as well) which codes for retinal rod-specific ABCR protein is responsible for Stargardt macular dystrophy/fundus flavimaculatus, an autosomal recessive macular dystrophy with juvenile onset, which accounts for 7% of human retinal degenerative diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP610669.RAsmSYYJ6K9apNbbxsUCbitkygBBsrsVM9xX_I9Tc9Ybo130_provenance.
- NP330111.RAdDs5pFgf1LO9FTcgPNuDRKMNcbkFsD4uUPwe9kZLI8c130_assertion description "[For example, mutations in the ABCR gene, (recently identified in cones as well) which codes for retinal rod-specific ABCR protein is responsible for Stargardt macular dystrophy/fundus flavimaculatus, an autosomal recessive macular dystrophy with juvenile onset, which accounts for 7% of human retinal degenerative diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP330111.RAdDs5pFgf1LO9FTcgPNuDRKMNcbkFsD4uUPwe9kZLI8c130_provenance.
- NP330109.RAKgVGnkGH5r9JtwKLhvJFVQsrvv3C2xyWRJA6-WYc0yA130_assertion description "[For example, mutations in the ABCR gene, (recently identified in cones as well) which codes for retinal rod-specific ABCR protein is responsible for Stargardt macular dystrophy/fundus flavimaculatus, an autosomal recessive macular dystrophy with juvenile onset, which accounts for 7% of human retinal degenerative diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP330109.RAKgVGnkGH5r9JtwKLhvJFVQsrvv3C2xyWRJA6-WYc0yA130_provenance.
- NP330116.RA5MOVLR1OwLBLk_svfJj44bfZvHINwXs16fqufuB1yOk130_assertion description "[For example, mutations in the ABCR gene, (recently identified in cones as well) which codes for retinal rod-specific ABCR protein is responsible for Stargardt macular dystrophy/fundus flavimaculatus, an autosomal recessive macular dystrophy with juvenile onset, which accounts for 7% of human retinal degenerative diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP330116.RA5MOVLR1OwLBLk_svfJj44bfZvHINwXs16fqufuB1yOk130_provenance.