Matches in Nanopublications for { ?s ?p "[This is the third reported mutation in CERKL causing retinal degeneration but is the first report to show that a single amino acid change in CERKL, rather than a null mutation, can cause retinal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 12 of
12
with 100 items per page.
- NP893752.RAYWr5JCBizyXQ4pOxcxP0WAyyeAXkdkGA1fEmxhA91i8130_assertion description "[This is the third reported mutation in CERKL causing retinal degeneration but is the first report to show that a single amino acid change in CERKL, rather than a null mutation, can cause retinal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP893752.RAYWr5JCBizyXQ4pOxcxP0WAyyeAXkdkGA1fEmxhA91i8130_provenance.
- NP718415.RAWKhtIcynDAvIgirBis87f9DR8ownTnEbJp7TYRVX610130_assertion description "[This is the third reported mutation in CERKL causing retinal degeneration but is the first report to show that a single amino acid change in CERKL, rather than a null mutation, can cause retinal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718415.RAWKhtIcynDAvIgirBis87f9DR8ownTnEbJp7TYRVX610130_provenance.
- NP120795.RA_wr50lTkq3P5l5-U2V0U_2jWYVCQMr6s2utg8OfSf90130_assertion description "[This is the third reported mutation in CERKL causing retinal degeneration but is the first report to show that a single amino acid change in CERKL, rather than a null mutation, can cause retinal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120795.RA_wr50lTkq3P5l5-U2V0U_2jWYVCQMr6s2utg8OfSf90130_provenance.
- NP122218.RAxeOvRJpsj2w-vTrb1KBz82ziZUwWvzs7VjkFVPYQWQg130_assertion description "[This is the third reported mutation in CERKL causing retinal degeneration but is the first report to show that a single amino acid change in CERKL, rather than a null mutation, can cause retinal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP122218.RAxeOvRJpsj2w-vTrb1KBz82ziZUwWvzs7VjkFVPYQWQg130_provenance.
- NP183986.RAWHPXSyOqMuluGWUNaysJHNvVVEOD2nvRHH5Hvllw1yc130_assertion description "[This is the third reported mutation in CERKL causing retinal degeneration but is the first report to show that a single amino acid change in CERKL, rather than a null mutation, can cause retinal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP183986.RAWHPXSyOqMuluGWUNaysJHNvVVEOD2nvRHH5Hvllw1yc130_provenance.
- NP185406.RATVMJGlB27yJcKT-j5do3beiQLE7OLaRhhlV7yKjRqvE130_assertion description "[This is the third reported mutation in CERKL causing retinal degeneration but is the first report to show that a single amino acid change in CERKL, rather than a null mutation, can cause retinal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185406.RATVMJGlB27yJcKT-j5do3beiQLE7OLaRhhlV7yKjRqvE130_provenance.
- assertion description "[This is the third reported mutation in CERKL causing retinal degeneration but is the first report to show that a single amino acid change in CERKL, rather than a null mutation, can cause retinal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[This is the third reported mutation in CERKL causing retinal degeneration but is the first report to show that a single amino acid change in CERKL, rather than a null mutation, can cause retinal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP701250.RAYKkXP_6UH5PXQZeu2vmuECuOoVBRCFlZtE-lWRYXgKk130_assertion description "[This is the third reported mutation in CERKL causing retinal degeneration but is the first report to show that a single amino acid change in CERKL, rather than a null mutation, can cause retinal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP701250.RAYKkXP_6UH5PXQZeu2vmuECuOoVBRCFlZtE-lWRYXgKk130_provenance.
- NP243350.RAuEU5Fee_Jfn0jcc4-fvFDkHTX9m1oo3MPirBiLhVXAI130_assertion description "[This is the third reported mutation in CERKL causing retinal degeneration but is the first report to show that a single amino acid change in CERKL, rather than a null mutation, can cause retinal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP243350.RAuEU5Fee_Jfn0jcc4-fvFDkHTX9m1oo3MPirBiLhVXAI130_provenance.
- NP988711.RAjuhKXr1SjKh1WVXaygwJtslyU369TpYykBTZ-C-_4BM130_assertion description "[This is the third reported mutation in CERKL causing retinal degeneration but is the first report to show that a single amino acid change in CERKL, rather than a null mutation, can cause retinal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988711.RAjuhKXr1SjKh1WVXaygwJtslyU369TpYykBTZ-C-_4BM130_provenance.
- NP243351.RAOQUq5khHF2UcIn7qB8nDBgQZOK19ZsIC30kGfzONmII130_assertion description "[This is the third reported mutation in CERKL causing retinal degeneration but is the first report to show that a single amino acid change in CERKL, rather than a null mutation, can cause retinal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP243351.RAOQUq5khHF2UcIn7qB8nDBgQZOK19ZsIC30kGfzONmII130_provenance.