Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP585916.RAcdAnaTRj05JWKv2nL_BfrFGnA2CdZDwYpuQlPXqSzEw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP585916.RAcdAnaTRj05JWKv2nL_BfrFGnA2CdZDwYpuQlPXqSzEw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP585916.RAcdAnaTRj05JWKv2nL_BfrFGnA2CdZDwYpuQlPXqSzEw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP585916.RAcdAnaTRj05JWKv2nL_BfrFGnA2CdZDwYpuQlPXqSzEw130_provenance.
- NP585916.RAcdAnaTRj05JWKv2nL_BfrFGnA2CdZDwYpuQlPXqSzEw130_assertion description "[The ND1 subunit gene of the mitochondrial NADH-ubiquinone oxidoreductase (complex I) is a hot spot for mutations causing Leber hereditary optic neuropathy and several mutations causing the mitochondrial encephalopathy, lactic acidosis and stroke-like episodes syndrome (MELAS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP585916.RAcdAnaTRj05JWKv2nL_BfrFGnA2CdZDwYpuQlPXqSzEw130_provenance.
- NP585916.RAcdAnaTRj05JWKv2nL_BfrFGnA2CdZDwYpuQlPXqSzEw130_assertion evidence source_evidence_literature NP585916.RAcdAnaTRj05JWKv2nL_BfrFGnA2CdZDwYpuQlPXqSzEw130_provenance.
- NP585916.RAcdAnaTRj05JWKv2nL_BfrFGnA2CdZDwYpuQlPXqSzEw130_assertion SIO_000772 16849371 NP585916.RAcdAnaTRj05JWKv2nL_BfrFGnA2CdZDwYpuQlPXqSzEw130_provenance.
- NP585916.RAcdAnaTRj05JWKv2nL_BfrFGnA2CdZDwYpuQlPXqSzEw130_assertion wasDerivedFrom befree-20150227 NP585916.RAcdAnaTRj05JWKv2nL_BfrFGnA2CdZDwYpuQlPXqSzEw130_provenance.
- NP585916.RAcdAnaTRj05JWKv2nL_BfrFGnA2CdZDwYpuQlPXqSzEw130_assertion wasGeneratedBy ECO_0000203 NP585916.RAcdAnaTRj05JWKv2nL_BfrFGnA2CdZDwYpuQlPXqSzEw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP585916.RAcdAnaTRj05JWKv2nL_BfrFGnA2CdZDwYpuQlPXqSzEw130_provenance.