Matches in Nanopublications for { ?s ?p "[OPA1 mutations are responsible for more than half of autosomal dominant optic atrophy (ADOA), a blinding disease affecting the retinal ganglion neurons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[OPA1 mutations are responsible for more than half of autosomal dominant optic atrophy (ADOA), a blinding disease affecting the retinal ganglion neurons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1260122.RAa9eEGY0CrWiJbof7OiAYboPmi4NKUG6zWvkwBKZfhmw130_assertion description "[OPA1 mutations are responsible for more than half of autosomal dominant optic atrophy (ADOA), a blinding disease affecting the retinal ganglion neurons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260122.RAa9eEGY0CrWiJbof7OiAYboPmi4NKUG6zWvkwBKZfhmw130_provenance.
- NP1260127.RAXhE4AcTAP2KLJG03C0DU9d7OWb-O0AtRSmAZQ24_kpQ130_assertion description "[OPA1 mutations are responsible for more than half of autosomal dominant optic atrophy (ADOA), a blinding disease affecting the retinal ganglion neurons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260127.RAXhE4AcTAP2KLJG03C0DU9d7OWb-O0AtRSmAZQ24_kpQ130_provenance.
- NP1260128.RAqR9lYpzBpGUEAKj1QlfYi0SI0paET8ixnRS91DkhZm8130_assertion description "[OPA1 mutations are responsible for more than half of autosomal dominant optic atrophy (ADOA), a blinding disease affecting the retinal ganglion neurons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260128.RAqR9lYpzBpGUEAKj1QlfYi0SI0paET8ixnRS91DkhZm8130_provenance.
- NP1260130.RAj53hQttnVJzM2EfOVzDenSN5fzP6k1RwDwE7wnStw6M130_assertion description "[OPA1 mutations are responsible for more than half of autosomal dominant optic atrophy (ADOA), a blinding disease affecting the retinal ganglion neurons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260130.RAj53hQttnVJzM2EfOVzDenSN5fzP6k1RwDwE7wnStw6M130_provenance.
- NP1260121.RA9WLJ0TIMDmZRVr7CyeQkY0eRxrEMDlK6Yo3m1S772e8130_assertion description "[OPA1 mutations are responsible for more than half of autosomal dominant optic atrophy (ADOA), a blinding disease affecting the retinal ganglion neurons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260121.RA9WLJ0TIMDmZRVr7CyeQkY0eRxrEMDlK6Yo3m1S772e8130_provenance.
- NP1260126.RAyW-9YOysxW1GfBzPeTFOlOZtKf1elzVi0TjdJfmV5ZI130_assertion description "[OPA1 mutations are responsible for more than half of autosomal dominant optic atrophy (ADOA), a blinding disease affecting the retinal ganglion neurons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260126.RAyW-9YOysxW1GfBzPeTFOlOZtKf1elzVi0TjdJfmV5ZI130_provenance.