Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP892500.RAFuKvuCv6nS3DEb6BIR_8kizwvwg3khZ6KcJA3ftqb2A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP892500.RAFuKvuCv6nS3DEb6BIR_8kizwvwg3khZ6KcJA3ftqb2A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP892500.RAFuKvuCv6nS3DEb6BIR_8kizwvwg3khZ6KcJA3ftqb2A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP892500.RAFuKvuCv6nS3DEb6BIR_8kizwvwg3khZ6KcJA3ftqb2A130_provenance.
- NP892500.RAFuKvuCv6nS3DEb6BIR_8kizwvwg3khZ6KcJA3ftqb2A130_assertion description "[Heterozygous optic atrophy type1 (OPA1) mutations are responsible for dominant optic atrophy, and the down regulation of OPA1 expression in patients with Leber hereditary optic neuropathy may imply that Opa1 protein levels in mitochondria play a role in other spontaneous optic neuropathies as well.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP892500.RAFuKvuCv6nS3DEb6BIR_8kizwvwg3khZ6KcJA3ftqb2A130_provenance.
- NP892500.RAFuKvuCv6nS3DEb6BIR_8kizwvwg3khZ6KcJA3ftqb2A130_assertion evidence source_evidence_literature NP892500.RAFuKvuCv6nS3DEb6BIR_8kizwvwg3khZ6KcJA3ftqb2A130_provenance.
- NP892500.RAFuKvuCv6nS3DEb6BIR_8kizwvwg3khZ6KcJA3ftqb2A130_assertion SIO_000772 21552501 NP892500.RAFuKvuCv6nS3DEb6BIR_8kizwvwg3khZ6KcJA3ftqb2A130_provenance.
- NP892500.RAFuKvuCv6nS3DEb6BIR_8kizwvwg3khZ6KcJA3ftqb2A130_assertion wasDerivedFrom befree-2016 NP892500.RAFuKvuCv6nS3DEb6BIR_8kizwvwg3khZ6KcJA3ftqb2A130_provenance.
- NP892500.RAFuKvuCv6nS3DEb6BIR_8kizwvwg3khZ6KcJA3ftqb2A130_assertion wasGeneratedBy ECO_0000203 NP892500.RAFuKvuCv6nS3DEb6BIR_8kizwvwg3khZ6KcJA3ftqb2A130_provenance.
- befree-2016 importedOn "2016-02-19" NP892500.RAFuKvuCv6nS3DEb6BIR_8kizwvwg3khZ6KcJA3ftqb2A130_provenance.