Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP343230.RAWlCywCO0qmCoFC4QostXODgAq1l4W0LUESE0czif1Jc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP343230.RAWlCywCO0qmCoFC4QostXODgAq1l4W0LUESE0czif1Jc130_assertion type Assertion NP343230.RAWlCywCO0qmCoFC4QostXODgAq1l4W0LUESE0czif1Jc130_head.
- 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.
- NP343230.RAWlCywCO0qmCoFC4QostXODgAq1l4W0LUESE0czif1Jc130_assertion evidence source_evidence_literature NP343230.RAWlCywCO0qmCoFC4QostXODgAq1l4W0LUESE0czif1Jc130_provenance.
- NP343230.RAWlCywCO0qmCoFC4QostXODgAq1l4W0LUESE0czif1Jc130_assertion SIO_000772 11810270 NP343230.RAWlCywCO0qmCoFC4QostXODgAq1l4W0LUESE0czif1Jc130_provenance.
- NP343230.RAWlCywCO0qmCoFC4QostXODgAq1l4W0LUESE0czif1Jc130_assertion wasDerivedFrom befree-2016 NP343230.RAWlCywCO0qmCoFC4QostXODgAq1l4W0LUESE0czif1Jc130_provenance.
- NP343230.RAWlCywCO0qmCoFC4QostXODgAq1l4W0LUESE0czif1Jc130_assertion wasGeneratedBy ECO_0000203 NP343230.RAWlCywCO0qmCoFC4QostXODgAq1l4W0LUESE0czif1Jc130_provenance.