Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP6350.RAQrZW9z-f2OV6HQMwisYUgoBh3csB7WhbgUQvyZgGANM130_assertion> ?p ?o ?g. }
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- NP6350.RAQrZW9z-f2OV6HQMwisYUgoBh3csB7WhbgUQvyZgGANM130_assertion type Assertion NP6350.RAQrZW9z-f2OV6HQMwisYUgoBh3csB7WhbgUQvyZgGANM130_head.
- NP6350.RAQrZW9z-f2OV6HQMwisYUgoBh3csB7WhbgUQvyZgGANM130_assertion description "[High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6350.RAQrZW9z-f2OV6HQMwisYUgoBh3csB7WhbgUQvyZgGANM130_provenance.
- NP6350.RAQrZW9z-f2OV6HQMwisYUgoBh3csB7WhbgUQvyZgGANM130_assertion evidence source_evidence_curated NP6350.RAQrZW9z-f2OV6HQMwisYUgoBh3csB7WhbgUQvyZgGANM130_provenance.
- NP6350.RAQrZW9z-f2OV6HQMwisYUgoBh3csB7WhbgUQvyZgGANM130_assertion SIO_000772 20818383 NP6350.RAQrZW9z-f2OV6HQMwisYUgoBh3csB7WhbgUQvyZgGANM130_provenance.
- NP6350.RAQrZW9z-f2OV6HQMwisYUgoBh3csB7WhbgUQvyZgGANM130_assertion wasDerivedFrom uniprot-2016 NP6350.RAQrZW9z-f2OV6HQMwisYUgoBh3csB7WhbgUQvyZgGANM130_provenance.
- NP6350.RAQrZW9z-f2OV6HQMwisYUgoBh3csB7WhbgUQvyZgGANM130_assertion wasGeneratedBy ECO_0000218 NP6350.RAQrZW9z-f2OV6HQMwisYUgoBh3csB7WhbgUQvyZgGANM130_provenance.