Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1260130.RAj53hQttnVJzM2EfOVzDenSN5fzP6k1RwDwE7wnStw6M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1260130.RAj53hQttnVJzM2EfOVzDenSN5fzP6k1RwDwE7wnStw6M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1260130.RAj53hQttnVJzM2EfOVzDenSN5fzP6k1RwDwE7wnStw6M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1260130.RAj53hQttnVJzM2EfOVzDenSN5fzP6k1RwDwE7wnStw6M130_provenance.
- NP1260130.RAj53hQttnVJzM2EfOVzDenSN5fzP6k1RwDwE7wnStw6M130_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." NP1260130.RAj53hQttnVJzM2EfOVzDenSN5fzP6k1RwDwE7wnStw6M130_provenance.
- NP1260130.RAj53hQttnVJzM2EfOVzDenSN5fzP6k1RwDwE7wnStw6M130_assertion evidence source_evidence_literature NP1260130.RAj53hQttnVJzM2EfOVzDenSN5fzP6k1RwDwE7wnStw6M130_provenance.
- NP1260130.RAj53hQttnVJzM2EfOVzDenSN5fzP6k1RwDwE7wnStw6M130_assertion SIO_000772 25641387 NP1260130.RAj53hQttnVJzM2EfOVzDenSN5fzP6k1RwDwE7wnStw6M130_provenance.
- NP1260130.RAj53hQttnVJzM2EfOVzDenSN5fzP6k1RwDwE7wnStw6M130_assertion wasDerivedFrom befree-2016 NP1260130.RAj53hQttnVJzM2EfOVzDenSN5fzP6k1RwDwE7wnStw6M130_provenance.
- NP1260130.RAj53hQttnVJzM2EfOVzDenSN5fzP6k1RwDwE7wnStw6M130_assertion wasGeneratedBy ECO_0000203 NP1260130.RAj53hQttnVJzM2EfOVzDenSN5fzP6k1RwDwE7wnStw6M130_provenance.
- befree-2016 importedOn "2016-02-19" NP1260130.RAj53hQttnVJzM2EfOVzDenSN5fzP6k1RwDwE7wnStw6M130_provenance.