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- source_evidence_literature type ECO_0000212 NP931389.RAbhQZxpezMTlIoygk-6Eb6w7bnAuWHCw3sBOX4CokI34130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP931389.RAbhQZxpezMTlIoygk-6Eb6w7bnAuWHCw3sBOX4CokI34130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP931389.RAbhQZxpezMTlIoygk-6Eb6w7bnAuWHCw3sBOX4CokI34130_provenance.
- NP931389.RAbhQZxpezMTlIoygk-6Eb6w7bnAuWHCw3sBOX4CokI34130_assertion wasGeneratedBy ECO_0000203 NP931389.RAbhQZxpezMTlIoygk-6Eb6w7bnAuWHCw3sBOX4CokI34130_provenance.
- NP931389.RAbhQZxpezMTlIoygk-6Eb6w7bnAuWHCw3sBOX4CokI34130_assertion wasDerivedFrom befree-20140225 NP931389.RAbhQZxpezMTlIoygk-6Eb6w7bnAuWHCw3sBOX4CokI34130_provenance.
- NP931389.RAbhQZxpezMTlIoygk-6Eb6w7bnAuWHCw3sBOX4CokI34130_assertion SIO_000772 19805825 NP931389.RAbhQZxpezMTlIoygk-6Eb6w7bnAuWHCw3sBOX4CokI34130_provenance.
- NP931389.RAbhQZxpezMTlIoygk-6Eb6w7bnAuWHCw3sBOX4CokI34130_assertion evidence source_evidence_literature NP931389.RAbhQZxpezMTlIoygk-6Eb6w7bnAuWHCw3sBOX4CokI34130_provenance.
- NP931389.RAbhQZxpezMTlIoygk-6Eb6w7bnAuWHCw3sBOX4CokI34130_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." NP931389.RAbhQZxpezMTlIoygk-6Eb6w7bnAuWHCw3sBOX4CokI34130_provenance.
- befree-20140225 importedOn "2014-02-25" NP931389.RAbhQZxpezMTlIoygk-6Eb6w7bnAuWHCw3sBOX4CokI34130_provenance.