Matches in Nanopublications for { ?s ?p "[Mutations in the retina-specific ATP-binding cassette transporter gene (ABCR) cause recessive Stargardt's disease (STGD) and fundus flavimaculatus (FFM), and were also found in 16% of patients with AMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Mutations in the retina-specific ATP-binding cassette transporter gene (ABCR) cause recessive Stargardt's disease (STGD) and fundus flavimaculatus (FFM), and were also found in 16% of patients with AMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP328311.RAVxO7Uu3feJr-NZD1m6MP2bZMd5IiFabEXlzJHGkBBrk130_assertion description "[Mutations in the retina-specific ATP-binding cassette transporter gene (ABCR) cause recessive Stargardt's disease (STGD) and fundus flavimaculatus (FFM), and were also found in 16% of patients with AMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP328311.RAVxO7Uu3feJr-NZD1m6MP2bZMd5IiFabEXlzJHGkBBrk130_provenance.
- NP1407859.RAUTm22dTRQG5RBo6FLB6gHjp41ooz1yRPgKmT-Dz2svc130_assertion description "[Mutations in the retina-specific ATP-binding cassette transporter gene (ABCR) cause recessive Stargardt's disease (STGD) and fundus flavimaculatus (FFM), and were also found in 16% of patients with AMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1407859.RAUTm22dTRQG5RBo6FLB6gHjp41ooz1yRPgKmT-Dz2svc130_provenance.