Matches in Nanopublications for { ?s ?p "[Optic atrophy type 1 (OPA1, MIM 165500) is a dominantly inherited optic neuropathy that features low visual acuity leading in many cases to legal blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 10 of
10
with 100 items per page.
- NP833560.RAUsjnBShWZJusTFT_VZQA9R4Bhy1OMGZ29HR3FkQaHhw130_assertion description "[Optic atrophy type 1 (OPA1, MIM 165500) is a dominantly inherited optic neuropathy that features low visual acuity leading in many cases to legal blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP833560.RAUsjnBShWZJusTFT_VZQA9R4Bhy1OMGZ29HR3FkQaHhw130_provenance.
- assertion description "[Optic atrophy type 1 (OPA1, MIM 165500) is a dominantly inherited optic neuropathy that features low visual acuity leading in many cases to legal blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Optic atrophy type 1 (OPA1, MIM 165500) is a dominantly inherited optic neuropathy that features low visual acuity leading in many cases to legal blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP602669.RAsxavg-F82ZxWz4HanhGReRckWqLUXeZ-iZ67v1jwTvY130_assertion description "[Optic atrophy type 1 (OPA1, MIM 165500) is a dominantly inherited optic neuropathy that features low visual acuity leading in many cases to legal blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP602669.RAsxavg-F82ZxWz4HanhGReRckWqLUXeZ-iZ67v1jwTvY130_provenance.
- NP343230.RAWlCywCO0qmCoFC4QostXODgAq1l4W0LUESE0czif1Jc130_assertion description "[Optic atrophy type 1 (OPA1, MIM 165500) is a dominantly inherited optic neuropathy that features low visual acuity leading in many cases to legal blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343230.RAWlCywCO0qmCoFC4QostXODgAq1l4W0LUESE0czif1Jc130_provenance.
- NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_assertion description "[Optic atrophy type 1 (OPA1, MIM 165500) is a dominantly inherited optic neuropathy that features low visual acuity leading in many cases to legal blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_provenance.
- NP833598.RAqXHelnXocN4UQqCH_q5bH0zEbhe_IbDTMr7dYhxwwCY130_assertion description "[Optic atrophy type 1 (OPA1, MIM 165500) is a dominantly inherited optic neuropathy that features low visual acuity leading in many cases to legal blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP833598.RAqXHelnXocN4UQqCH_q5bH0zEbhe_IbDTMr7dYhxwwCY130_provenance.
- NP343231.RAhXth2V_WMux76omZZwbdu5ppB28J_vOLGpQlz4zAsmU130_assertion description "[Optic atrophy type 1 (OPA1, MIM 165500) is a dominantly inherited optic neuropathy that features low visual acuity leading in many cases to legal blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343231.RAhXth2V_WMux76omZZwbdu5ppB28J_vOLGpQlz4zAsmU130_provenance.
- NP602703.RAIYV72MBzJYTZxnjpmwmgK1Ta98wzV8Y2j0raYIT4M6k130_assertion description "[Optic atrophy type 1 (OPA1, MIM 165500) is a dominantly inherited optic neuropathy that features low visual acuity leading in many cases to legal blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP602703.RAIYV72MBzJYTZxnjpmwmgK1Ta98wzV8Y2j0raYIT4M6k130_provenance.
- NP343229.RAEYyYO-cY9bkc6nBCyefke2IjRY9Wlt6q1M9VIp52A-A130_assertion description "[Optic atrophy type 1 (OPA1, MIM 165500) is a dominantly inherited optic neuropathy that features low visual acuity leading in many cases to legal blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343229.RAEYyYO-cY9bkc6nBCyefke2IjRY9Wlt6q1M9VIp52A-A130_provenance.