Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP720639.RA-XHWAAcndXDo6u1k2unSHIvmF8JUPEuu14XbdRbJIfs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP720639.RA-XHWAAcndXDo6u1k2unSHIvmF8JUPEuu14XbdRbJIfs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP720639.RA-XHWAAcndXDo6u1k2unSHIvmF8JUPEuu14XbdRbJIfs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP720639.RA-XHWAAcndXDo6u1k2unSHIvmF8JUPEuu14XbdRbJIfs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP720639.RA-XHWAAcndXDo6u1k2unSHIvmF8JUPEuu14XbdRbJIfs130_provenance.
- NP720639.RA-XHWAAcndXDo6u1k2unSHIvmF8JUPEuu14XbdRbJIfs130_assertion wasGeneratedBy ECO_0000203 NP720639.RA-XHWAAcndXDo6u1k2unSHIvmF8JUPEuu14XbdRbJIfs130_provenance.
- NP720639.RA-XHWAAcndXDo6u1k2unSHIvmF8JUPEuu14XbdRbJIfs130_assertion wasDerivedFrom befree-20150227 NP720639.RA-XHWAAcndXDo6u1k2unSHIvmF8JUPEuu14XbdRbJIfs130_provenance.
- NP720639.RA-XHWAAcndXDo6u1k2unSHIvmF8JUPEuu14XbdRbJIfs130_assertion SIO_000772 19805825 NP720639.RA-XHWAAcndXDo6u1k2unSHIvmF8JUPEuu14XbdRbJIfs130_provenance.
- NP720639.RA-XHWAAcndXDo6u1k2unSHIvmF8JUPEuu14XbdRbJIfs130_assertion evidence source_evidence_literature NP720639.RA-XHWAAcndXDo6u1k2unSHIvmF8JUPEuu14XbdRbJIfs130_provenance.
- NP720639.RA-XHWAAcndXDo6u1k2unSHIvmF8JUPEuu14XbdRbJIfs130_assertion description "[Mutations in the nuclear SURF-1 gene lead directly to cytochrome-c oxidase deficiency, the most common respiratory chain defect in Leigh syndrome, a neurodegenerative mitochondrial disease involving the deep gray matter and brain stem.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP720639.RA-XHWAAcndXDo6u1k2unSHIvmF8JUPEuu14XbdRbJIfs130_provenance.