Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1260121.RA9WLJ0TIMDmZRVr7CyeQkY0eRxrEMDlK6Yo3m1S772e8130_assertion> ?p ?o ?g. }
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- NP1260121.RA9WLJ0TIMDmZRVr7CyeQkY0eRxrEMDlK6Yo3m1S772e8130_assertion type Assertion NP1260121.RA9WLJ0TIMDmZRVr7CyeQkY0eRxrEMDlK6Yo3m1S772e8130_head.
- NP1260121.RA9WLJ0TIMDmZRVr7CyeQkY0eRxrEMDlK6Yo3m1S772e8130_assertion description "[OPA1 mutations are responsible for more than half of autosomal dominant optic atrophy (ADOA), a blinding disease affecting the retinal ganglion neurons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260121.RA9WLJ0TIMDmZRVr7CyeQkY0eRxrEMDlK6Yo3m1S772e8130_provenance.
- NP1260121.RA9WLJ0TIMDmZRVr7CyeQkY0eRxrEMDlK6Yo3m1S772e8130_assertion evidence source_evidence_literature NP1260121.RA9WLJ0TIMDmZRVr7CyeQkY0eRxrEMDlK6Yo3m1S772e8130_provenance.
- NP1260121.RA9WLJ0TIMDmZRVr7CyeQkY0eRxrEMDlK6Yo3m1S772e8130_assertion SIO_000772 25641387 NP1260121.RA9WLJ0TIMDmZRVr7CyeQkY0eRxrEMDlK6Yo3m1S772e8130_provenance.
- NP1260121.RA9WLJ0TIMDmZRVr7CyeQkY0eRxrEMDlK6Yo3m1S772e8130_assertion wasDerivedFrom befree-2016 NP1260121.RA9WLJ0TIMDmZRVr7CyeQkY0eRxrEMDlK6Yo3m1S772e8130_provenance.
- NP1260121.RA9WLJ0TIMDmZRVr7CyeQkY0eRxrEMDlK6Yo3m1S772e8130_assertion wasGeneratedBy ECO_0000203 NP1260121.RA9WLJ0TIMDmZRVr7CyeQkY0eRxrEMDlK6Yo3m1S772e8130_provenance.