Matches in Nanopublications for { ?s ?p "[Due to the unique role of 11-cis retinol dehydrogenase in the generation of visual pigments, it is a candidate gene for involvement in hereditary eye disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 3 of
3
with 100 items per page.
- NP661483.RA86z_OLCnXeEYivHKB3hw-ehh3By4Bq7i-oU474z_JGs130_assertion description "[Due to the unique role of 11-cis retinol dehydrogenase in the generation of visual pigments, it is a candidate gene for involvement in hereditary eye disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP661483.RA86z_OLCnXeEYivHKB3hw-ehh3By4Bq7i-oU474z_JGs130_provenance.
- NP668468.RAf3BjpzX9wy5Jkf8YKUXqeHnPHCAYzgeGiL_CUhEPOrY130_assertion description "[Due to the unique role of 11-cis retinol dehydrogenase in the generation of visual pigments, it is a candidate gene for involvement in hereditary eye disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668468.RAf3BjpzX9wy5Jkf8YKUXqeHnPHCAYzgeGiL_CUhEPOrY130_provenance.
- NP1360947.RAg9f5bvo-OMwkqkSrjp7xFTtbE5iZgxqu8X8UiE9p5gY130_assertion description "[Due to the unique role of 11-cis retinol dehydrogenase in the generation of visual pigments, it is a candidate gene for involvement in hereditary eye disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1360947.RAg9f5bvo-OMwkqkSrjp7xFTtbE5iZgxqu8X8UiE9p5gY130_provenance.