Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP602703.RAIYV72MBzJYTZxnjpmwmgK1Ta98wzV8Y2j0raYIT4M6k130_assertion> ?p ?o ?g. }
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- NP602703.RAIYV72MBzJYTZxnjpmwmgK1Ta98wzV8Y2j0raYIT4M6k130_assertion type Assertion NP602703.RAIYV72MBzJYTZxnjpmwmgK1Ta98wzV8Y2j0raYIT4M6k130_head.
- 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.
- NP602703.RAIYV72MBzJYTZxnjpmwmgK1Ta98wzV8Y2j0raYIT4M6k130_assertion evidence source_evidence_literature NP602703.RAIYV72MBzJYTZxnjpmwmgK1Ta98wzV8Y2j0raYIT4M6k130_provenance.
- NP602703.RAIYV72MBzJYTZxnjpmwmgK1Ta98wzV8Y2j0raYIT4M6k130_assertion SIO_000772 11810270 NP602703.RAIYV72MBzJYTZxnjpmwmgK1Ta98wzV8Y2j0raYIT4M6k130_provenance.
- NP602703.RAIYV72MBzJYTZxnjpmwmgK1Ta98wzV8Y2j0raYIT4M6k130_assertion wasDerivedFrom befree-20150227 NP602703.RAIYV72MBzJYTZxnjpmwmgK1Ta98wzV8Y2j0raYIT4M6k130_provenance.
- NP602703.RAIYV72MBzJYTZxnjpmwmgK1Ta98wzV8Y2j0raYIT4M6k130_assertion wasGeneratedBy ECO_0000203 NP602703.RAIYV72MBzJYTZxnjpmwmgK1Ta98wzV8Y2j0raYIT4M6k130_provenance.