Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP95407.RAsh2p1Z7WsQjNjfdKqmwe8RLIEgmaaljyI-Cvkr0Mepg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP95407.RAsh2p1Z7WsQjNjfdKqmwe8RLIEgmaaljyI-Cvkr0Mepg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP95407.RAsh2p1Z7WsQjNjfdKqmwe8RLIEgmaaljyI-Cvkr0Mepg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP95407.RAsh2p1Z7WsQjNjfdKqmwe8RLIEgmaaljyI-Cvkr0Mepg130_provenance.
- NP95407.RAsh2p1Z7WsQjNjfdKqmwe8RLIEgmaaljyI-Cvkr0Mepg130_assertion description "[Leber hereditary optic neuropathy (LHON) is one of the most common mitochondrial diseases, which is mainly caused by three mitochondrial DNA (mtDNA) mutations (m.3460G>A, m.11778G>A and m.14484T>C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95407.RAsh2p1Z7WsQjNjfdKqmwe8RLIEgmaaljyI-Cvkr0Mepg130_provenance.
- NP95407.RAsh2p1Z7WsQjNjfdKqmwe8RLIEgmaaljyI-Cvkr0Mepg130_assertion evidence source_evidence_literature NP95407.RAsh2p1Z7WsQjNjfdKqmwe8RLIEgmaaljyI-Cvkr0Mepg130_provenance.
- NP95407.RAsh2p1Z7WsQjNjfdKqmwe8RLIEgmaaljyI-Cvkr0Mepg130_assertion SIO_000772 20599858 NP95407.RAsh2p1Z7WsQjNjfdKqmwe8RLIEgmaaljyI-Cvkr0Mepg130_provenance.
- NP95407.RAsh2p1Z7WsQjNjfdKqmwe8RLIEgmaaljyI-Cvkr0Mepg130_assertion wasDerivedFrom gad-20150221 NP95407.RAsh2p1Z7WsQjNjfdKqmwe8RLIEgmaaljyI-Cvkr0Mepg130_provenance.
- NP95407.RAsh2p1Z7WsQjNjfdKqmwe8RLIEgmaaljyI-Cvkr0Mepg130_assertion wasGeneratedBy ECO_0000203 NP95407.RAsh2p1Z7WsQjNjfdKqmwe8RLIEgmaaljyI-Cvkr0Mepg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP95407.RAsh2p1Z7WsQjNjfdKqmwe8RLIEgmaaljyI-Cvkr0Mepg130_provenance.