Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP770021.RAoHpipZj3x3Fxdgh4Sokii3nk-ak3QaAkxOtSql6pGdw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP770021.RAoHpipZj3x3Fxdgh4Sokii3nk-ak3QaAkxOtSql6pGdw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP770021.RAoHpipZj3x3Fxdgh4Sokii3nk-ak3QaAkxOtSql6pGdw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP770021.RAoHpipZj3x3Fxdgh4Sokii3nk-ak3QaAkxOtSql6pGdw130_provenance.
- NP770021.RAoHpipZj3x3Fxdgh4Sokii3nk-ak3QaAkxOtSql6pGdw130_assertion description "[Two genes for dominantly inherited optic atrophy have been mapped (OPA1 and OPA4), of which the gene has been identified in one (OPA1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP770021.RAoHpipZj3x3Fxdgh4Sokii3nk-ak3QaAkxOtSql6pGdw130_provenance.
- NP770021.RAoHpipZj3x3Fxdgh4Sokii3nk-ak3QaAkxOtSql6pGdw130_assertion evidence source_evidence_literature NP770021.RAoHpipZj3x3Fxdgh4Sokii3nk-ak3QaAkxOtSql6pGdw130_provenance.
- NP770021.RAoHpipZj3x3Fxdgh4Sokii3nk-ak3QaAkxOtSql6pGdw130_assertion SIO_000772 15534598 NP770021.RAoHpipZj3x3Fxdgh4Sokii3nk-ak3QaAkxOtSql6pGdw130_provenance.
- NP770021.RAoHpipZj3x3Fxdgh4Sokii3nk-ak3QaAkxOtSql6pGdw130_assertion wasDerivedFrom befree-20140225 NP770021.RAoHpipZj3x3Fxdgh4Sokii3nk-ak3QaAkxOtSql6pGdw130_provenance.
- NP770021.RAoHpipZj3x3Fxdgh4Sokii3nk-ak3QaAkxOtSql6pGdw130_assertion wasGeneratedBy ECO_0000203 NP770021.RAoHpipZj3x3Fxdgh4Sokii3nk-ak3QaAkxOtSql6pGdw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP770021.RAoHpipZj3x3Fxdgh4Sokii3nk-ak3QaAkxOtSql6pGdw130_provenance.