Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP16162.RA9_E7rFmEOPQ_yH48cCVywp8IAX6qP5PpKBJzxyD6jdE130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP16162.RA9_E7rFmEOPQ_yH48cCVywp8IAX6qP5PpKBJzxyD6jdE130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP16162.RA9_E7rFmEOPQ_yH48cCVywp8IAX6qP5PpKBJzxyD6jdE130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP16162.RA9_E7rFmEOPQ_yH48cCVywp8IAX6qP5PpKBJzxyD6jdE130_provenance.
- NP16162.RA9_E7rFmEOPQ_yH48cCVywp8IAX6qP5PpKBJzxyD6jdE130_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." NP16162.RA9_E7rFmEOPQ_yH48cCVywp8IAX6qP5PpKBJzxyD6jdE130_provenance.
- NP16162.RA9_E7rFmEOPQ_yH48cCVywp8IAX6qP5PpKBJzxyD6jdE130_assertion evidence source_evidence_curated NP16162.RA9_E7rFmEOPQ_yH48cCVywp8IAX6qP5PpKBJzxyD6jdE130_provenance.
- NP16162.RA9_E7rFmEOPQ_yH48cCVywp8IAX6qP5PpKBJzxyD6jdE130_assertion SIO_000772 20858599 NP16162.RA9_E7rFmEOPQ_yH48cCVywp8IAX6qP5PpKBJzxyD6jdE130_provenance.
- NP16162.RA9_E7rFmEOPQ_yH48cCVywp8IAX6qP5PpKBJzxyD6jdE130_assertion wasDerivedFrom ctd_human-20130708 NP16162.RA9_E7rFmEOPQ_yH48cCVywp8IAX6qP5PpKBJzxyD6jdE130_provenance.
- NP16162.RA9_E7rFmEOPQ_yH48cCVywp8IAX6qP5PpKBJzxyD6jdE130_assertion wasGeneratedBy ECO_0000218 NP16162.RA9_E7rFmEOPQ_yH48cCVywp8IAX6qP5PpKBJzxyD6jdE130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP16162.RA9_E7rFmEOPQ_yH48cCVywp8IAX6qP5PpKBJzxyD6jdE130_provenance.