Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_provenance.
• NP3253.RAQBcj9ES9t1ibEhQHqR3dbKrF42uPmGMShn0x5u86ztY130_assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3253.RAQBcj9ES9t1ibEhQHqR3dbKrF42uPmGMShn0x5u86ztY130_provenance.
• NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_provenance.
• NP1009197.RABLdsF5yTG_9JgONV4GPyRVumj1wcMURdfq95U7ML_ig130_assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1009197.RABLdsF5yTG_9JgONV4GPyRVumj1wcMURdfq95U7ML_ig130_provenance.
• NP528881.RAAvUJK2NuwbArAsv-PRgeEOo4d7piY2h-8tSU3jsmT5U130_assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528881.RAAvUJK2NuwbArAsv-PRgeEOo4d7piY2h-8tSU3jsmT5U130_provenance.
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• NP19457.RAkvkirJlbBMskIUm8Rw_EP0HnzHJkoq4UBnYznhC9T2U130_assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP19457.RAkvkirJlbBMskIUm8Rw_EP0HnzHJkoq4UBnYznhC9T2U130_provenance.
• NP528882.RA8B-EBL82nkNqIi8Kj4mCtjSIU_CGaZ5-jPWSR0q6Jvc130_assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528882.RA8B-EBL82nkNqIi8Kj4mCtjSIU_CGaZ5-jPWSR0q6Jvc130_provenance.
• NP4334.RAW_-M_Rm6k9QamtQHxIatUzXBhFlQArNc4IMi2nnI2Ro130_assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4334.RAW_-M_Rm6k9QamtQHxIatUzXBhFlQArNc4IMi2nnI2Ro130_provenance.
• NP16855.RAe3O3cbe4tWCxGNo4s9mmX0cxbWPU8jF-g4A3TUREAhw130_assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP16855.RAe3O3cbe4tWCxGNo4s9mmX0cxbWPU8jF-g4A3TUREAhw130_provenance.
• assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP528886.RAGFuShptAhhxmZ0m452wjJ0BRWGbX0k6mgBUdvwY40FI130_assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528886.RAGFuShptAhhxmZ0m452wjJ0BRWGbX0k6mgBUdvwY40FI130_provenance.
• NP4333.RAOClorgkkGrJEdokzXjHmP3KGNWsNCq6gqVEk_HP7b9E130_assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4333.RAOClorgkkGrJEdokzXjHmP3KGNWsNCq6gqVEk_HP7b9E130_provenance.
• NP1009201.RALjLV8VYMSA15f1TQMCso-Q_6BnkRLytuFHJW1A1E4Lw130_assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1009201.RALjLV8VYMSA15f1TQMCso-Q_6BnkRLytuFHJW1A1E4Lw130_provenance.
• NP16854.RAHpJPklk5bI3ffze_dcvzWKffukLbptO8jD8vKkL8LSw130_assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP16854.RAHpJPklk5bI3ffze_dcvzWKffukLbptO8jD8vKkL8LSw130_provenance.
• NP509543.RAvcULs-ayIwQCR0_lEUwfbeBBNjoXfkTKcTJpGDBgVh0130_assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP509543.RAvcULs-ayIwQCR0_lEUwfbeBBNjoXfkTKcTJpGDBgVh0130_provenance.
• NP509549.RAk8QIaxPEOii0oWNkntDuFav-uwmxfdNgXnx8WT-YgaE130_assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP509549.RAk8QIaxPEOii0oWNkntDuFav-uwmxfdNgXnx8WT-YgaE130_provenance.