Matches in Nanopublications for { ?s ?p "[Mutations in the CNGA3 gene have been associated with complete and incomplete forms of total colour blindness (achromatopsia), a disorder characterized by reduced visual acuity, lack of colour discrimination, photophobia and nystagmus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP812348.RAWrcOeJYTR1cACLW6tF5n57y-02xxnVWcJer-ZSpJPew130_assertion description "[Mutations in the CNGA3 gene have been associated with complete and incomplete forms of total colour blindness (achromatopsia), a disorder characterized by reduced visual acuity, lack of colour discrimination, photophobia and nystagmus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP812348.RAWrcOeJYTR1cACLW6tF5n57y-02xxnVWcJer-ZSpJPew130_provenance.
- NP233967.RA07RsQtMkktU501WN1LN8U_im0kL8RH70HpbpOnFKQdM130_assertion description "[Mutations in the CNGA3 gene have been associated with complete and incomplete forms of total colour blindness (achromatopsia), a disorder characterized by reduced visual acuity, lack of colour discrimination, photophobia and nystagmus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP233967.RA07RsQtMkktU501WN1LN8U_im0kL8RH70HpbpOnFKQdM130_provenance.
- assertion description "[Mutations in the CNGA3 gene have been associated with complete and incomplete forms of total colour blindness (achromatopsia), a disorder characterized by reduced visual acuity, lack of colour discrimination, photophobia and nystagmus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in the CNGA3 gene have been associated with complete and incomplete forms of total colour blindness (achromatopsia), a disorder characterized by reduced visual acuity, lack of colour discrimination, photophobia and nystagmus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP318342.RAZwx5VOOiH_xOHCD5Hf4Ai5_4MaxcFV02UjP2icjCqKw130_assertion description "[Mutations in the CNGA3 gene have been associated with complete and incomplete forms of total colour blindness (achromatopsia), a disorder characterized by reduced visual acuity, lack of colour discrimination, photophobia and nystagmus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP318342.RAZwx5VOOiH_xOHCD5Hf4Ai5_4MaxcFV02UjP2icjCqKw130_provenance.
- NP668475.RAwFLUeNFN33xRPJtKP6JgM7OH00QQM_Vp1NJYPi1Gm7U130_assertion description "[Mutations in the CNGA3 gene have been associated with complete and incomplete forms of total colour blindness (achromatopsia), a disorder characterized by reduced visual acuity, lack of colour discrimination, photophobia and nystagmus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668475.RAwFLUeNFN33xRPJtKP6JgM7OH00QQM_Vp1NJYPi1Gm7U130_provenance.