Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP516031.RA_7iP5giyHrAOXx4Z5DDThpxFM4gokkp_icBhj1Bm1cQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP516031.RA_7iP5giyHrAOXx4Z5DDThpxFM4gokkp_icBhj1Bm1cQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP516031.RA_7iP5giyHrAOXx4Z5DDThpxFM4gokkp_icBhj1Bm1cQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP516031.RA_7iP5giyHrAOXx4Z5DDThpxFM4gokkp_icBhj1Bm1cQ130_provenance.
- NP516031.RA_7iP5giyHrAOXx4Z5DDThpxFM4gokkp_icBhj1Bm1cQ130_assertion description "[NADH:ubiquinone oxidoreductase (complex I) deficiency is a common cause of mitochondrial oxidative phosphorylation disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP516031.RA_7iP5giyHrAOXx4Z5DDThpxFM4gokkp_icBhj1Bm1cQ130_provenance.
- NP516031.RA_7iP5giyHrAOXx4Z5DDThpxFM4gokkp_icBhj1Bm1cQ130_assertion evidence source_evidence_literature NP516031.RA_7iP5giyHrAOXx4Z5DDThpxFM4gokkp_icBhj1Bm1cQ130_provenance.
- NP516031.RA_7iP5giyHrAOXx4Z5DDThpxFM4gokkp_icBhj1Bm1cQ130_assertion SIO_000772 16200211 NP516031.RA_7iP5giyHrAOXx4Z5DDThpxFM4gokkp_icBhj1Bm1cQ130_provenance.
- NP516031.RA_7iP5giyHrAOXx4Z5DDThpxFM4gokkp_icBhj1Bm1cQ130_assertion wasDerivedFrom befree-2016 NP516031.RA_7iP5giyHrAOXx4Z5DDThpxFM4gokkp_icBhj1Bm1cQ130_provenance.
- NP516031.RA_7iP5giyHrAOXx4Z5DDThpxFM4gokkp_icBhj1Bm1cQ130_assertion wasGeneratedBy ECO_0000203 NP516031.RA_7iP5giyHrAOXx4Z5DDThpxFM4gokkp_icBhj1Bm1cQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP516031.RA_7iP5giyHrAOXx4Z5DDThpxFM4gokkp_icBhj1Bm1cQ130_provenance.