Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP323016.RADzE6kOxPWZrJqndiE4MRvqWOV-idUaydYfPj3XH9hBE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP323016.RADzE6kOxPWZrJqndiE4MRvqWOV-idUaydYfPj3XH9hBE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP323016.RADzE6kOxPWZrJqndiE4MRvqWOV-idUaydYfPj3XH9hBE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP323016.RADzE6kOxPWZrJqndiE4MRvqWOV-idUaydYfPj3XH9hBE130_provenance.
- NP323016.RADzE6kOxPWZrJqndiE4MRvqWOV-idUaydYfPj3XH9hBE130_assertion description "[Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323016.RADzE6kOxPWZrJqndiE4MRvqWOV-idUaydYfPj3XH9hBE130_provenance.
- NP323016.RADzE6kOxPWZrJqndiE4MRvqWOV-idUaydYfPj3XH9hBE130_assertion evidence source_evidence_literature NP323016.RADzE6kOxPWZrJqndiE4MRvqWOV-idUaydYfPj3XH9hBE130_provenance.
- NP323016.RADzE6kOxPWZrJqndiE4MRvqWOV-idUaydYfPj3XH9hBE130_assertion SIO_000772 11440989 NP323016.RADzE6kOxPWZrJqndiE4MRvqWOV-idUaydYfPj3XH9hBE130_provenance.
- NP323016.RADzE6kOxPWZrJqndiE4MRvqWOV-idUaydYfPj3XH9hBE130_assertion wasDerivedFrom befree-2016 NP323016.RADzE6kOxPWZrJqndiE4MRvqWOV-idUaydYfPj3XH9hBE130_provenance.
- NP323016.RADzE6kOxPWZrJqndiE4MRvqWOV-idUaydYfPj3XH9hBE130_assertion wasGeneratedBy ECO_0000203 NP323016.RADzE6kOxPWZrJqndiE4MRvqWOV-idUaydYfPj3XH9hBE130_provenance.
- befree-2016 importedOn "2016-02-19" NP323016.RADzE6kOxPWZrJqndiE4MRvqWOV-idUaydYfPj3XH9hBE130_provenance.