Matches in Nanopublications for { ?s ?p "[A mutation in this gene causes X-linked cone dystrophy/type of hereditary retinal degeneration is distinct from retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP122220.RAn8RCjYSG25w0QfrcX_Hi3fwqSfCTeD-QxOBtkaQKnys130_assertion description "[A mutation in this gene causes X-linked cone dystrophy/type of hereditary retinal degeneration is distinct from retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP122220.RAn8RCjYSG25w0QfrcX_Hi3fwqSfCTeD-QxOBtkaQKnys130_provenance.
- NP122319.RALS4iFWHgqfRzcM4_-btga9TlZchzbULLJR9-4QlDkdY130_assertion description "[A mutation in this gene causes X-linked cone dystrophy/type of hereditary retinal degeneration is distinct from retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP122319.RALS4iFWHgqfRzcM4_-btga9TlZchzbULLJR9-4QlDkdY130_provenance.
- assertion description "[A mutation in this gene causes X-linked cone dystrophy/type of hereditary retinal degeneration is distinct from retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[A mutation in this gene causes X-linked cone dystrophy/type of hereditary retinal degeneration is distinct from retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP185506.RAtdWYLfLYvcpvF9JMlm4LpFD_VAEtYD7JcZJQ4KHf8zA130_assertion description "[A mutation in this gene causes X-linked cone dystrophy/type of hereditary retinal degeneration is distinct from retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185506.RAtdWYLfLYvcpvF9JMlm4LpFD_VAEtYD7JcZJQ4KHf8zA130_provenance.
- NP193496.RAWpvWeSGijD7dhLa9MTiHZlOWrbrVuOoprEIj6qJYXGw130_assertion description "[A mutation in this gene causes X-linked cone dystrophy/type of hereditary retinal degeneration is distinct from retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193496.RAWpvWeSGijD7dhLa9MTiHZlOWrbrVuOoprEIj6qJYXGw130_provenance.
- NP185408.RAwvMK2_A4c8Zgapd4rzzzEvXr6KbtFfpRgsW2a19UHSc130_assertion description "[A mutation in this gene causes X-linked cone dystrophy/type of hereditary retinal degeneration is distinct from retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185408.RAwvMK2_A4c8Zgapd4rzzzEvXr6KbtFfpRgsW2a19UHSc130_provenance.
- NP193495.RA8b1a4slUbISKgztX9NMZtU6LZ6BMK4CPMf-4bIMlXrE130_assertion description "[A mutation in this gene causes X-linked cone dystrophy/type of hereditary retinal degeneration is distinct from retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193495.RA8b1a4slUbISKgztX9NMZtU6LZ6BMK4CPMf-4bIMlXrE130_provenance.