Matches in Nanopublications for { ?s ?p "[Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP6750.RAI24YvNIsPlSiI-44rlcNEhYCHqRkYfqS9frnR5ANaYk130_assertion description "[Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6750.RAI24YvNIsPlSiI-44rlcNEhYCHqRkYfqS9frnR5ANaYk130_provenance.
- NP3987.RAdZIS8_djqOcPHjkOrwv060wkhT3GA7IfZBo2hSUqpvA130_assertion description "[Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3987.RAdZIS8_djqOcPHjkOrwv060wkhT3GA7IfZBo2hSUqpvA130_provenance.
- NP666509.RA6MeXfOSQnE2pWKxHmRp00wZX2eMqglWkK9dqon3MCXw130_assertion description "[Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP666509.RA6MeXfOSQnE2pWKxHmRp00wZX2eMqglWkK9dqon3MCXw130_provenance.
- NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_assertion description "[Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_provenance.
- assertion description "[Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP559872.RAH1pTbdJj2ndrE1rDPKKCKa3xRgCAY6yPKbdtdoinbBM130_assertion description "[Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP559872.RAH1pTbdJj2ndrE1rDPKKCKa3xRgCAY6yPKbdtdoinbBM130_provenance.
- NP5979.RArauR6mZV2RzwWQH_iPTet89ScEPqZ0_P87NsF_gf8DY130_assertion description "[Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5979.RArauR6mZV2RzwWQH_iPTet89ScEPqZ0_P87NsF_gf8DY130_provenance.