Matches in Nanopublications for { ?s ?p "[Missense mutations in NRL are associated with autosomal dominant retinitis pigmentosa; however, the phenotype associated with the loss of NRL function in humans has not been reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP916988.RAng1Du_-6nOlRDmXQxxchVE2oGNEhvK0xTVfOIW34U0c130_assertion description "[Missense mutations in NRL are associated with autosomal dominant retinitis pigmentosa; however, the phenotype associated with the loss of NRL function in humans has not been reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP916988.RAng1Du_-6nOlRDmXQxxchVE2oGNEhvK0xTVfOIW34U0c130_provenance.
- assertion description "[Missense mutations in NRL are associated with autosomal dominant retinitis pigmentosa; however, the phenotype associated with the loss of NRL function in humans has not been reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP599175.RAiKJsm041tv5wkcuSHn5-VeV-K4BK8HPDaffx670T6Ho130_assertion description "[Missense mutations in NRL are associated with autosomal dominant retinitis pigmentosa; however, the phenotype associated with the loss of NRL function in humans has not been reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP599175.RAiKJsm041tv5wkcuSHn5-VeV-K4BK8HPDaffx670T6Ho130_provenance.
- NP472222.RA8SRj4M672TIiLKVplxWt4a0ffUbP-YoaVJ3cIpuLP0w130_assertion description "[Missense mutations in NRL are associated with autosomal dominant retinitis pigmentosa; however, the phenotype associated with the loss of NRL function in humans has not been reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP472222.RA8SRj4M672TIiLKVplxWt4a0ffUbP-YoaVJ3cIpuLP0w130_provenance.