Matches in Nanopublications for { ?s ?p "[To examine the phenotypes of 8 patients with evidence of cone dysfunction and normal color vision (characteristic features of both oligocone trichromacy and bradyopsia), and subsequently to screen RGS9 and R9AP for disease-causing mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP220439.RAIpX4ztO1xZNQ1lBmCGL9cLiD5heqLEueZZSJz0WjdWg130_assertion description "[To examine the phenotypes of 8 patients with evidence of cone dysfunction and normal color vision (characteristic features of both oligocone trichromacy and bradyopsia), and subsequently to screen RGS9 and R9AP for disease-causing mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220439.RAIpX4ztO1xZNQ1lBmCGL9cLiD5heqLEueZZSJz0WjdWg130_provenance.
- assertion description "[To examine the phenotypes of 8 patients with evidence of cone dysfunction and normal color vision (characteristic features of both oligocone trichromacy and bradyopsia), and subsequently to screen RGS9 and R9AP for disease-causing mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[To examine the phenotypes of 8 patients with evidence of cone dysfunction and normal color vision (characteristic features of both oligocone trichromacy and bradyopsia), and subsequently to screen RGS9 and R9AP for disease-causing mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.