Matches in Nanopublications for { ?s ?p "[OPA1, the gene responsible for autosomal dominant optic atrophy represents an excellent candidate gene for NTG, as the clinical phenotypes are similar and OPA1 is expressed in the retina and optic nerve.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[OPA1, the gene responsible for autosomal dominant optic atrophy represents an excellent candidate gene for NTG, as the clinical phenotypes are similar and OPA1 is expressed in the retina and optic nerve.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP343262.RAaHt3dDcZttKbR8p29Sfn-nahDp_4klrHsPuiPiZ7HC0130_assertion description "[OPA1, the gene responsible for autosomal dominant optic atrophy represents an excellent candidate gene for NTG, as the clinical phenotypes are similar and OPA1 is expressed in the retina and optic nerve.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343262.RAaHt3dDcZttKbR8p29Sfn-nahDp_4klrHsPuiPiZ7HC0130_provenance.
- NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_assertion description "[OPA1, the gene responsible for autosomal dominant optic atrophy represents an excellent candidate gene for NTG, as the clinical phenotypes are similar and OPA1 is expressed in the retina and optic nerve.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_provenance.