Matches in Nanopublications for { ?s ?p "[Earlier, the peripherin/RDS Arg-172-Trp mutation was associated primarily with a macular degeneration phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP328008.RAfXI_T8CEKqqUWwg0tW3trL33zk8ynn5BxLURXGLuZkw130_assertion description "[Earlier, the peripherin/RDS Arg-172-Trp mutation was associated primarily with a macular degeneration phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP328008.RAfXI_T8CEKqqUWwg0tW3trL33zk8ynn5BxLURXGLuZkw130_provenance.
- NP478165.RAQO2ooGxD6MkA-FK0tiOT0oblJ_sfbZFPkRdmbpymMLo130_assertion description "[Earlier, the peripherin/RDS Arg-172-Trp mutation was associated primarily with a macular degeneration phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478165.RAQO2ooGxD6MkA-FK0tiOT0oblJ_sfbZFPkRdmbpymMLo130_provenance.
- NP426856.RAypNZlrWKGXYbvEzkgNjMsejQ2QEYjxpeIgMuJ16RNbU130_assertion description "[Earlier, the peripherin/RDS Arg-172-Trp mutation was associated primarily with a macular degeneration phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426856.RAypNZlrWKGXYbvEzkgNjMsejQ2QEYjxpeIgMuJ16RNbU130_provenance.
- NP421940.RASnZYPwTvCALFFZjwgOLXaN9-r9mN9480sob4BN_FuX8130_assertion description "[Earlier, the peripherin/RDS Arg-172-Trp mutation was associated primarily with a macular degeneration phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP421940.RASnZYPwTvCALFFZjwgOLXaN9-r9mN9480sob4BN_FuX8130_provenance.
- NP649180.RAUAbf_fU9lmZsy8snIC4comUEyWjZYsRXpbKh7WYuNR8130_assertion description "[Earlier, the peripherin/RDS Arg-172-Trp mutation was associated primarily with a macular degeneration phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649180.RAUAbf_fU9lmZsy8snIC4comUEyWjZYsRXpbKh7WYuNR8130_provenance.
- assertion description "[Earlier, the peripherin/RDS Arg-172-Trp mutation was associated primarily with a macular degeneration phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1407864.RAfdyWj7vrBZuqGBhQQsfz56u3Xz2DkeUMz575JtM-Hx4130_assertion description "[Earlier, the peripherin/RDS Arg-172-Trp mutation was associated primarily with a macular degeneration phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1407864.RAfdyWj7vrBZuqGBhQQsfz56u3Xz2DkeUMz575JtM-Hx4130_provenance.
- NP1407862.RAD-qrA00uDZq8HrF3Cn9eAjvNDFS4557Mh35md17wMbk130_assertion description "[Earlier, the peripherin/RDS Arg-172-Trp mutation was associated primarily with a macular degeneration phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1407862.RAD-qrA00uDZq8HrF3Cn9eAjvNDFS4557Mh35md17wMbk130_provenance.
- NP668526.RA25jwm9PlFeB7XRKdCH0R9sCtT0BE0A2GTVS3ieEMZcs130_assertion description "[Earlier, the peripherin/RDS Arg-172-Trp mutation was associated primarily with a macular degeneration phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668526.RA25jwm9PlFeB7XRKdCH0R9sCtT0BE0A2GTVS3ieEMZcs130_provenance.
- NP1407867.RAPm7RVnPCtH4WXJrWnTSaxNcNcFV-KLk9Rh3BuTZ_rw0130_assertion description "[Earlier, the peripherin/RDS Arg-172-Trp mutation was associated primarily with a macular degeneration phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1407867.RAPm7RVnPCtH4WXJrWnTSaxNcNcFV-KLk9Rh3BuTZ_rw0130_provenance.
- NP1407863.RA7_0-SAfsK4P16K0eEkIyM0ulQPBl8Sw0vsH4cRyUOi0130_assertion description "[Earlier, the peripherin/RDS Arg-172-Trp mutation was associated primarily with a macular degeneration phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1407863.RA7_0-SAfsK4P16K0eEkIyM0ulQPBl8Sw0vsH4cRyUOi0130_provenance.