Matches in Nanopublications for { ?s ?p "[The retinal degeneration in this patient is most likely to be secondary to a genetic disorder of autosomal or X-linked recessive inheritance rather than SCA6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP276985.RAV1xvnGl9S7NAOvOwdnr9gyyz8YmheCQw_CJDDd6KbpI130_assertion description "[The retinal degeneration in this patient is most likely to be secondary to a genetic disorder of autosomal or X-linked recessive inheritance rather than SCA6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276985.RAV1xvnGl9S7NAOvOwdnr9gyyz8YmheCQw_CJDDd6KbpI130_provenance.
- NP277020.RAX38OqdBBh4DiC-Hzu9E2g1EljVr5kE5wKf3CwiR_noc130_assertion description "[The retinal degeneration in this patient is most likely to be secondary to a genetic disorder of autosomal or X-linked recessive inheritance rather than SCA6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277020.RAX38OqdBBh4DiC-Hzu9E2g1EljVr5kE5wKf3CwiR_noc130_provenance.
- NP664177.RA2QIU-jW5hA2oGYt-bhIV4RwGTgi8iBFol9qvNiFMv5Y130_assertion description "[The retinal degeneration in this patient is most likely to be secondary to a genetic disorder of autosomal or X-linked recessive inheritance rather than SCA6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP664177.RA2QIU-jW5hA2oGYt-bhIV4RwGTgi8iBFol9qvNiFMv5Y130_provenance.
- NP580720.RALNoylApJrQWq7EgK9-O5SSxqLqswqRfyG9cdRKvRfn8130_assertion description "[The retinal degeneration in this patient is most likely to be secondary to a genetic disorder of autosomal or X-linked recessive inheritance rather than SCA6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP580720.RALNoylApJrQWq7EgK9-O5SSxqLqswqRfyG9cdRKvRfn8130_provenance.
- NP358608.RAsndbo7kCMlCIhR40B-UCNDENZJ0G8YfJWyAfnLAhMJ4130_assertion description "[The retinal degeneration in this patient is most likely to be secondary to a genetic disorder of autosomal or X-linked recessive inheritance rather than SCA6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP358608.RAsndbo7kCMlCIhR40B-UCNDENZJ0G8YfJWyAfnLAhMJ4130_provenance.