Matches in Nanopublications for { ?s ?p "[To investigate functional abnormalities in mutations in the peripherin (RDS) gene leading to different clinical types of autosomal dominant retinal disease--macular degeneration and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 17 of
17
with 100 items per page.
- NP552068.RAgF8Yy8_osow4Tr5BZ1Euq3Lhtr_ivSrM6tJla5U7ID8130_assertion description "[To investigate functional abnormalities in mutations in the peripherin (RDS) gene leading to different clinical types of autosomal dominant retinal disease--macular degeneration and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP552068.RAgF8Yy8_osow4Tr5BZ1Euq3Lhtr_ivSrM6tJla5U7ID8130_provenance.
- NP346986.RAC5B3maN_6BWjQ5Aspl-cvY2z3Aw7xjqTBB3DiHTu-WA130_assertion description "[To investigate functional abnormalities in mutations in the peripherin (RDS) gene leading to different clinical types of autosomal dominant retinal disease--macular degeneration and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP346986.RAC5B3maN_6BWjQ5Aspl-cvY2z3Aw7xjqTBB3DiHTu-WA130_provenance.
- NP868912.RAUu0HGR1gUCCse6U_v40nK6hnQB6uuERQ_auXZ9TZcfk130_assertion description "[To investigate functional abnormalities in mutations in the peripherin (RDS) gene leading to different clinical types of autosomal dominant retinal disease--macular degeneration and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868912.RAUu0HGR1gUCCse6U_v40nK6hnQB6uuERQ_auXZ9TZcfk130_provenance.
- NP709868.RAniqdNS5P99vxFXaI1kXgbYxQZDoQCrqB5fhu6txFrYo130_assertion description "[To investigate functional abnormalities in mutations in the peripherin (RDS) gene leading to different clinical types of autosomal dominant retinal disease--macular degeneration and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP709868.RAniqdNS5P99vxFXaI1kXgbYxQZDoQCrqB5fhu6txFrYo130_provenance.
- NP283999.RA-y60Oa3ft8nnq0alfRQpGkXGq5JjRC--h2LLX6LOkxQ130_assertion description "[To investigate functional abnormalities in mutations in the peripherin (RDS) gene leading to different clinical types of autosomal dominant retinal disease--macular degeneration and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP283999.RA-y60Oa3ft8nnq0alfRQpGkXGq5JjRC--h2LLX6LOkxQ130_provenance.
- NP668542.RAUPpCZQ5uK_kVe1YZ7S6kj88QjItPDk5h9LWU1ZxlVUc130_assertion description "[To investigate functional abnormalities in mutations in the peripherin (RDS) gene leading to different clinical types of autosomal dominant retinal disease--macular degeneration and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668542.RAUPpCZQ5uK_kVe1YZ7S6kj88QjItPDk5h9LWU1ZxlVUc130_provenance.
- NP649194.RAxsKR0lUNb6g_jlBP8DYBnX54tUDx_9cTFCM2RqrJxSE130_assertion description "[To investigate functional abnormalities in mutations in the peripherin (RDS) gene leading to different clinical types of autosomal dominant retinal disease--macular degeneration and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649194.RAxsKR0lUNb6g_jlBP8DYBnX54tUDx_9cTFCM2RqrJxSE130_provenance.
- NP1330673.RAZ0Gbeiw4RW5XWlt3kMAd1HuWgpLgwgXdgyAt-xTPrXE130_assertion description "[To investigate functional abnormalities in mutations in the peripherin (RDS) gene leading to different clinical types of autosomal dominant retinal disease--macular degeneration and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1330673.RAZ0Gbeiw4RW5XWlt3kMAd1HuWgpLgwgXdgyAt-xTPrXE130_provenance.
- assertion description "[To investigate functional abnormalities in mutations in the peripherin (RDS) gene leading to different clinical types of autosomal dominant retinal disease--macular degeneration and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[To investigate functional abnormalities in mutations in the peripherin (RDS) gene leading to different clinical types of autosomal dominant retinal disease--macular degeneration and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[To investigate functional abnormalities in mutations in the peripherin (RDS) gene leading to different clinical types of autosomal dominant retinal disease--macular degeneration and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[To investigate functional abnormalities in mutations in the peripherin (RDS) gene leading to different clinical types of autosomal dominant retinal disease--macular degeneration and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[To investigate functional abnormalities in mutations in the peripherin (RDS) gene leading to different clinical types of autosomal dominant retinal disease--macular degeneration and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1330676.RAo6m3UQP9K53FkZLPAVI5hROeewa1ok1RV2-e4ZxoXS0130_assertion description "[To investigate functional abnormalities in mutations in the peripherin (RDS) gene leading to different clinical types of autosomal dominant retinal disease--macular degeneration and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1330676.RAo6m3UQP9K53FkZLPAVI5hROeewa1ok1RV2-e4ZxoXS0130_provenance.
- NP1330681.RAgw4Vpa9_vTT6i-shzPNAndKzYfH-vOZ9KUivme3qF6Q130_assertion description "[To investigate functional abnormalities in mutations in the peripherin (RDS) gene leading to different clinical types of autosomal dominant retinal disease--macular degeneration and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1330681.RAgw4Vpa9_vTT6i-shzPNAndKzYfH-vOZ9KUivme3qF6Q130_provenance.
- NP1330682.RAPYAKcPk1k5FYeIBxYEl2YZCUUZTph05yiug3cdBDyk4130_assertion description "[To investigate functional abnormalities in mutations in the peripherin (RDS) gene leading to different clinical types of autosomal dominant retinal disease--macular degeneration and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1330682.RAPYAKcPk1k5FYeIBxYEl2YZCUUZTph05yiug3cdBDyk4130_provenance.
- NP760956.RAl3T2ndrJ75Wd-vM2M_JKwUn4VUZecJ4NTmPGAkLOboI130_assertion description "[To investigate functional abnormalities in mutations in the peripherin (RDS) gene leading to different clinical types of autosomal dominant retinal disease--macular degeneration and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP760956.RAl3T2ndrJ75Wd-vM2M_JKwUn4VUZecJ4NTmPGAkLOboI130_provenance.