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- source_evidence_literature type ECO_0000212 NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_provenance.
- NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_assertion description "[OPA1, the gene responsible for autosomal dominant optic atrophy represents an excellent candidate gene for NTG, as the clinical phenotypes are similar and OPA1 is expressed in the retina and optic nerve.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_provenance.
- NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_assertion evidence source_evidence_literature NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_provenance.
- NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_assertion SIO_000772 11810296 NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_provenance.
- NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_assertion wasDerivedFrom befree-2016 NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_provenance.
- NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_assertion wasGeneratedBy ECO_0000203 NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_provenance.
- befree-2016 importedOn "2016-02-19" NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_provenance.