Matches in Nanopublications for { ?s ?p "[Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP7081.RAzvEbqm6dlcg93Oim1eIjgRXcONTZ7wiAxpQv-QRWhF0130_assertion description "[Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7081.RAzvEbqm6dlcg93Oim1eIjgRXcONTZ7wiAxpQv-QRWhF0130_provenance.
- NP502599.RAGOvS6FAA96uBOqycJe2cwZ3mcVR2D4B-lwOw96taLoY130_assertion description "[Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP502599.RAGOvS6FAA96uBOqycJe2cwZ3mcVR2D4B-lwOw96taLoY130_provenance.
- assertion description "[Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP547526.RAb83SPU8y2s8uRcKhIQBIdv-RAI2XaSGfQ3w8WOBbl0g130_assertion description "[Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547526.RAb83SPU8y2s8uRcKhIQBIdv-RAI2XaSGfQ3w8WOBbl0g130_provenance.
- NP4497.RApMABcr2mFqHdQGYEMOt6WytQ9zsj5YCIZHDlXeoCfWQ130_assertion description "[Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4497.RApMABcr2mFqHdQGYEMOt6WytQ9zsj5YCIZHDlXeoCfWQ130_provenance.
- NP776954.RA2xSMxvM7YvjYaYOhGHLIPx9WxscHsIM7tkN2uL5nlyI130_assertion description "[Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776954.RA2xSMxvM7YvjYaYOhGHLIPx9WxscHsIM7tkN2uL5nlyI130_provenance.