Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP668807.RAHSmsOPeT2x3tYwWFtrZzZUo65b9FTjc_9Z2pDPWspnA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP668807.RAHSmsOPeT2x3tYwWFtrZzZUo65b9FTjc_9Z2pDPWspnA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668807.RAHSmsOPeT2x3tYwWFtrZzZUo65b9FTjc_9Z2pDPWspnA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668807.RAHSmsOPeT2x3tYwWFtrZzZUo65b9FTjc_9Z2pDPWspnA130_provenance.
- NP668807.RAHSmsOPeT2x3tYwWFtrZzZUo65b9FTjc_9Z2pDPWspnA130_assertion description "[Furthermore, during the last decade, it has been identified that mutations in two mitochondrial fusion genes (MFN2 and OPA1) cause prevalent neurodegenerative diseases (Charcot-Marie Tooth type 2A and Kjer disease/autosomal dominant optic atrophy).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668807.RAHSmsOPeT2x3tYwWFtrZzZUo65b9FTjc_9Z2pDPWspnA130_provenance.
- NP668807.RAHSmsOPeT2x3tYwWFtrZzZUo65b9FTjc_9Z2pDPWspnA130_assertion evidence source_evidence_literature NP668807.RAHSmsOPeT2x3tYwWFtrZzZUo65b9FTjc_9Z2pDPWspnA130_provenance.
- NP668807.RAHSmsOPeT2x3tYwWFtrZzZUo65b9FTjc_9Z2pDPWspnA130_assertion SIO_000772 19584314 NP668807.RAHSmsOPeT2x3tYwWFtrZzZUo65b9FTjc_9Z2pDPWspnA130_provenance.
- NP668807.RAHSmsOPeT2x3tYwWFtrZzZUo65b9FTjc_9Z2pDPWspnA130_assertion wasDerivedFrom befree-20140225 NP668807.RAHSmsOPeT2x3tYwWFtrZzZUo65b9FTjc_9Z2pDPWspnA130_provenance.
- NP668807.RAHSmsOPeT2x3tYwWFtrZzZUo65b9FTjc_9Z2pDPWspnA130_assertion wasGeneratedBy ECO_0000203 NP668807.RAHSmsOPeT2x3tYwWFtrZzZUo65b9FTjc_9Z2pDPWspnA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP668807.RAHSmsOPeT2x3tYwWFtrZzZUo65b9FTjc_9Z2pDPWspnA130_provenance.