Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_assertion> ?p ?o ?g. }
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- NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_assertion type Assertion NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_head.
- 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.
- NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_assertion evidence source_evidence_literature NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_provenance.
- NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_assertion SIO_000772 11810270 NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_provenance.
- NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_assertion wasDerivedFrom befree-2016 NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_provenance.
- NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_assertion wasGeneratedBy ECO_0000203 NP343232.RAcfPq-mdiqkvdHCW-Y2hXYZN7AIqIroCHLr6nSzKQe6Y130_provenance.