Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP26872.RAAyRwWVs1fPDKqxuY2lHBFtjM139H8hHdi_d3u6PkLFk130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP26872.RAAyRwWVs1fPDKqxuY2lHBFtjM139H8hHdi_d3u6PkLFk130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP26872.RAAyRwWVs1fPDKqxuY2lHBFtjM139H8hHdi_d3u6PkLFk130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP26872.RAAyRwWVs1fPDKqxuY2lHBFtjM139H8hHdi_d3u6PkLFk130_provenance.
- NP26872.RAAyRwWVs1fPDKqxuY2lHBFtjM139H8hHdi_d3u6PkLFk130_assertion description "[FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP26872.RAAyRwWVs1fPDKqxuY2lHBFtjM139H8hHdi_d3u6PkLFk130_provenance.
- NP26872.RAAyRwWVs1fPDKqxuY2lHBFtjM139H8hHdi_d3u6PkLFk130_assertion evidence source_evidence_curated NP26872.RAAyRwWVs1fPDKqxuY2lHBFtjM139H8hHdi_d3u6PkLFk130_provenance.
- NP26872.RAAyRwWVs1fPDKqxuY2lHBFtjM139H8hHdi_d3u6PkLFk130_assertion SIO_000772 20858599 NP26872.RAAyRwWVs1fPDKqxuY2lHBFtjM139H8hHdi_d3u6PkLFk130_provenance.
- NP26872.RAAyRwWVs1fPDKqxuY2lHBFtjM139H8hHdi_d3u6PkLFk130_assertion wasDerivedFrom ctd_human-2016 NP26872.RAAyRwWVs1fPDKqxuY2lHBFtjM139H8hHdi_d3u6PkLFk130_provenance.
- NP26872.RAAyRwWVs1fPDKqxuY2lHBFtjM139H8hHdi_d3u6PkLFk130_assertion wasGeneratedBy ECO_0000218 NP26872.RAAyRwWVs1fPDKqxuY2lHBFtjM139H8hHdi_d3u6PkLFk130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP26872.RAAyRwWVs1fPDKqxuY2lHBFtjM139H8hHdi_d3u6PkLFk130_provenance.