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- source_evidence_literature type ECO_0000212 NP763001.RA41JBWj_TyDBrZ3OgmXbL-WQKTMEN_eNX3zy3MkYHYBI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP763001.RA41JBWj_TyDBrZ3OgmXbL-WQKTMEN_eNX3zy3MkYHYBI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP763001.RA41JBWj_TyDBrZ3OgmXbL-WQKTMEN_eNX3zy3MkYHYBI130_provenance.
- NP763001.RA41JBWj_TyDBrZ3OgmXbL-WQKTMEN_eNX3zy3MkYHYBI130_assertion description "[Nicotinamide adenine dinucleotide (NADH):ubiquinone oxidoreductase (complex I) enzyme deficiencies account for a significant proportion of mitochondrial disorders, including LS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP763001.RA41JBWj_TyDBrZ3OgmXbL-WQKTMEN_eNX3zy3MkYHYBI130_provenance.
- NP763001.RA41JBWj_TyDBrZ3OgmXbL-WQKTMEN_eNX3zy3MkYHYBI130_assertion evidence source_evidence_literature NP763001.RA41JBWj_TyDBrZ3OgmXbL-WQKTMEN_eNX3zy3MkYHYBI130_provenance.
- NP763001.RA41JBWj_TyDBrZ3OgmXbL-WQKTMEN_eNX3zy3MkYHYBI130_assertion SIO_000772 23266820 NP763001.RA41JBWj_TyDBrZ3OgmXbL-WQKTMEN_eNX3zy3MkYHYBI130_provenance.
- NP763001.RA41JBWj_TyDBrZ3OgmXbL-WQKTMEN_eNX3zy3MkYHYBI130_assertion wasDerivedFrom befree-20150227 NP763001.RA41JBWj_TyDBrZ3OgmXbL-WQKTMEN_eNX3zy3MkYHYBI130_provenance.
- NP763001.RA41JBWj_TyDBrZ3OgmXbL-WQKTMEN_eNX3zy3MkYHYBI130_assertion wasGeneratedBy ECO_0000203 NP763001.RA41JBWj_TyDBrZ3OgmXbL-WQKTMEN_eNX3zy3MkYHYBI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP763001.RA41JBWj_TyDBrZ3OgmXbL-WQKTMEN_eNX3zy3MkYHYBI130_provenance.