Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[This finding and the previous findings of a 45% frequency of phenotypic color vision defects in patients with AMN may suggest that the ALD/AMN gene lies 5' to the red pigment gene and that the frequent phenotypic color vision anomalies owe their origin to deleted DNA that includes regulatory genes for color vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP907703.RAto0IJOf2bx0DKz6AldgzMAFAl2IHjsH4Zwg83H_ngiU130_assertion description "[This finding and the previous findings of a 45% frequency of phenotypic color vision defects in patients with AMN may suggest that the ALD/AMN gene lies 5' to the red pigment gene and that the frequent phenotypic color vision anomalies owe their origin to deleted DNA that includes regulatory genes for color vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP907703.RAto0IJOf2bx0DKz6AldgzMAFAl2IHjsH4Zwg83H_ngiU130_provenance.
• NP357579.RAxx8lWiTKNZppE3wKfm89TS79aRJbABP1rhBBBQt_2K0130_assertion description "[This finding and the previous findings of a 45% frequency of phenotypic color vision defects in patients with AMN may suggest that the ALD/AMN gene lies 5' to the red pigment gene and that the frequent phenotypic color vision anomalies owe their origin to deleted DNA that includes regulatory genes for color vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP357579.RAxx8lWiTKNZppE3wKfm89TS79aRJbABP1rhBBBQt_2K0130_provenance.
• NP171064.RAPfrAhlTEZZH82atAGbI05xfd9XhVDOWzV5U1cREcwks130_assertion description "[This finding and the previous findings of a 45% frequency of phenotypic color vision defects in patients with AMN may suggest that the ALD/AMN gene lies 5' to the red pigment gene and that the frequent phenotypic color vision anomalies owe their origin to deleted DNA that includes regulatory genes for color vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP171064.RAPfrAhlTEZZH82atAGbI05xfd9XhVDOWzV5U1cREcwks130_provenance.
• NP758554.RA7ZUL27_WcAdTwFKQrxFnSRmrMC2MoSA6xDcJgZobYh8130_assertion description "[This finding and the previous findings of a 45% frequency of phenotypic color vision defects in patients with AMN may suggest that the ALD/AMN gene lies 5' to the red pigment gene and that the frequent phenotypic color vision anomalies owe their origin to deleted DNA that includes regulatory genes for color vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP758554.RA7ZUL27_WcAdTwFKQrxFnSRmrMC2MoSA6xDcJgZobYh8130_provenance.
• NP1023653.RARTq3Izo_j0fUZkiGuarqvP23MbKfCd8U8WlVxi_-YLE130_assertion description "[This finding and the previous findings of a 45% frequency of phenotypic color vision defects in patients with AMN may suggest that the ALD/AMN gene lies 5' to the red pigment gene and that the frequent phenotypic color vision anomalies owe their origin to deleted DNA that includes regulatory genes for color vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1023653.RARTq3Izo_j0fUZkiGuarqvP23MbKfCd8U8WlVxi_-YLE130_provenance.
• NP951865.RAuvvXR6e9dXFJYgOYGfTC6iLrc1PVaRgEurBR4yaPnqo130_assertion description "[This finding and the previous findings of a 45% frequency of phenotypic color vision defects in patients with AMN may suggest that the ALD/AMN gene lies 5' to the red pigment gene and that the frequent phenotypic color vision anomalies owe their origin to deleted DNA that includes regulatory genes for color vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP951865.RAuvvXR6e9dXFJYgOYGfTC6iLrc1PVaRgEurBR4yaPnqo130_provenance.
• NP951873.RAgMJJfyBz4d9ffA_IWWPH2upwvU4vctJx7oCbmXiBYwE130_assertion description "[This finding and the previous findings of a 45% frequency of phenotypic color vision defects in patients with AMN may suggest that the ALD/AMN gene lies 5' to the red pigment gene and that the frequent phenotypic color vision anomalies owe their origin to deleted DNA that includes regulatory genes for color vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP951873.RAgMJJfyBz4d9ffA_IWWPH2upwvU4vctJx7oCbmXiBYwE130_provenance.
• assertion description "[This finding and the previous findings of a 45% frequency of phenotypic color vision defects in patients with AMN may suggest that the ALD/AMN gene lies 5' to the red pigment gene and that the frequent phenotypic color vision anomalies owe their origin to deleted DNA that includes regulatory genes for color vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[This finding and the previous findings of a 45% frequency of phenotypic color vision defects in patients with AMN may suggest that the ALD/AMN gene lies 5' to the red pigment gene and that the frequent phenotypic color vision anomalies owe their origin to deleted DNA that includes regulatory genes for color vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[This finding and the previous findings of a 45% frequency of phenotypic color vision defects in patients with AMN may suggest that the ALD/AMN gene lies 5' to the red pigment gene and that the frequent phenotypic color vision anomalies owe their origin to deleted DNA that includes regulatory genes for color vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[This finding and the previous findings of a 45% frequency of phenotypic color vision defects in patients with AMN may suggest that the ALD/AMN gene lies 5' to the red pigment gene and that the frequent phenotypic color vision anomalies owe their origin to deleted DNA that includes regulatory genes for color vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP1023650.RADgI3VaMGnn_CM4ksldj_R3K8jjmHoQZkSksWwozMdj0130_assertion description "[This finding and the previous findings of a 45% frequency of phenotypic color vision defects in patients with AMN may suggest that the ALD/AMN gene lies 5' to the red pigment gene and that the frequent phenotypic color vision anomalies owe their origin to deleted DNA that includes regulatory genes for color vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1023650.RADgI3VaMGnn_CM4ksldj_R3K8jjmHoQZkSksWwozMdj0130_provenance.
• NP1023651.RAD3-gfLRoIiFZHYglp1oKsUTt2jLr8yxlPMyw2eOU-6U130_assertion description "[This finding and the previous findings of a 45% frequency of phenotypic color vision defects in patients with AMN may suggest that the ALD/AMN gene lies 5' to the red pigment gene and that the frequent phenotypic color vision anomalies owe their origin to deleted DNA that includes regulatory genes for color vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1023651.RAD3-gfLRoIiFZHYglp1oKsUTt2jLr8yxlPMyw2eOU-6U130_provenance.
• NP1023649.RAsPEqD1J4-aOCs8vAh1ruyMrezGIgKRQ1h868fmmn7cU130_assertion description "[This finding and the previous findings of a 45% frequency of phenotypic color vision defects in patients with AMN may suggest that the ALD/AMN gene lies 5' to the red pigment gene and that the frequent phenotypic color vision anomalies owe their origin to deleted DNA that includes regulatory genes for color vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1023649.RAsPEqD1J4-aOCs8vAh1ruyMrezGIgKRQ1h868fmmn7cU130_provenance.
• NP1023652.RAmKRN1F1m6SHovpkWXHv3k-ySm0GhRutuyajI8nBOkrU130_assertion description "[This finding and the previous findings of a 45% frequency of phenotypic color vision defects in patients with AMN may suggest that the ALD/AMN gene lies 5' to the red pigment gene and that the frequent phenotypic color vision anomalies owe their origin to deleted DNA that includes regulatory genes for color vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1023652.RAmKRN1F1m6SHovpkWXHv3k-ySm0GhRutuyajI8nBOkrU130_provenance.
• NP234022.RAzKhN86ML_4f7aUQnZc6ubd-kFZ9VvZ_WQSsuzqEKpJA130_assertion description "[This finding and the previous findings of a 45% frequency of phenotypic color vision defects in patients with AMN may suggest that the ALD/AMN gene lies 5' to the red pigment gene and that the frequent phenotypic color vision anomalies owe their origin to deleted DNA that includes regulatory genes for color vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP234022.RAzKhN86ML_4f7aUQnZc6ubd-kFZ9VvZ_WQSsuzqEKpJA130_provenance.
• NP1023654.RAzlLUGlh6qWeBZXcg8y6vIw5udPNa5oFIeNcdIaxcQ9A130_assertion description "[This finding and the previous findings of a 45% frequency of phenotypic color vision defects in patients with AMN may suggest that the ALD/AMN gene lies 5' to the red pigment gene and that the frequent phenotypic color vision anomalies owe their origin to deleted DNA that includes regulatory genes for color vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1023654.RAzlLUGlh6qWeBZXcg8y6vIw5udPNa5oFIeNcdIaxcQ9A130_provenance.
• NP951883.RA-IKQbgNY4m1VStCobne6epQK9-BuekWAvxyrLcR5F7U130_assertion description "[This finding and the previous findings of a 45% frequency of phenotypic color vision defects in patients with AMN may suggest that the ALD/AMN gene lies 5' to the red pigment gene and that the frequent phenotypic color vision anomalies owe their origin to deleted DNA that includes regulatory genes for color vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP951883.RA-IKQbgNY4m1VStCobne6epQK9-BuekWAvxyrLcR5F7U130_provenance.