Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP224624.RAuX-aq2syAMZS9PlaNEv_ThEXMyXSCNEQAOEnHTFIlDU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP224624.RAuX-aq2syAMZS9PlaNEv_ThEXMyXSCNEQAOEnHTFIlDU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP224624.RAuX-aq2syAMZS9PlaNEv_ThEXMyXSCNEQAOEnHTFIlDU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP224624.RAuX-aq2syAMZS9PlaNEv_ThEXMyXSCNEQAOEnHTFIlDU130_provenance.
- NP224624.RAuX-aq2syAMZS9PlaNEv_ThEXMyXSCNEQAOEnHTFIlDU130_assertion wasGeneratedBy ECO_0000203 NP224624.RAuX-aq2syAMZS9PlaNEv_ThEXMyXSCNEQAOEnHTFIlDU130_provenance.
- NP224624.RAuX-aq2syAMZS9PlaNEv_ThEXMyXSCNEQAOEnHTFIlDU130_assertion wasDerivedFrom befree-20140225 NP224624.RAuX-aq2syAMZS9PlaNEv_ThEXMyXSCNEQAOEnHTFIlDU130_provenance.
- NP224624.RAuX-aq2syAMZS9PlaNEv_ThEXMyXSCNEQAOEnHTFIlDU130_assertion SIO_000772 18806273 NP224624.RAuX-aq2syAMZS9PlaNEv_ThEXMyXSCNEQAOEnHTFIlDU130_provenance.
- NP224624.RAuX-aq2syAMZS9PlaNEv_ThEXMyXSCNEQAOEnHTFIlDU130_assertion evidence source_evidence_literature NP224624.RAuX-aq2syAMZS9PlaNEv_ThEXMyXSCNEQAOEnHTFIlDU130_provenance.
- NP224624.RAuX-aq2syAMZS9PlaNEv_ThEXMyXSCNEQAOEnHTFIlDU130_assertion description "[Leber's hereditary optic neuropathy (LHON), the most frequent mitochondrial disorder, is mostly due to three mitochondrial DNA (mtDNA) mutations in respiratory chain complex I subunit genes: 3460/ND1, 11778/ND4 and 14484/ND6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP224624.RAuX-aq2syAMZS9PlaNEv_ThEXMyXSCNEQAOEnHTFIlDU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP224624.RAuX-aq2syAMZS9PlaNEv_ThEXMyXSCNEQAOEnHTFIlDU130_provenance.