Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP6353.RAbPcr5RtvOvt_qkOEqLM6i0NBgpb-_h9OAzJT3xKO6rQ130_assertion> ?p ?o ?g. }
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- NP6353.RAbPcr5RtvOvt_qkOEqLM6i0NBgpb-_h9OAzJT3xKO6rQ130_assertion type Assertion NP6353.RAbPcr5RtvOvt_qkOEqLM6i0NBgpb-_h9OAzJT3xKO6rQ130_head.
- NP6353.RAbPcr5RtvOvt_qkOEqLM6i0NBgpb-_h9OAzJT3xKO6rQ130_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." NP6353.RAbPcr5RtvOvt_qkOEqLM6i0NBgpb-_h9OAzJT3xKO6rQ130_provenance.
- NP6353.RAbPcr5RtvOvt_qkOEqLM6i0NBgpb-_h9OAzJT3xKO6rQ130_assertion evidence source_evidence_curated NP6353.RAbPcr5RtvOvt_qkOEqLM6i0NBgpb-_h9OAzJT3xKO6rQ130_provenance.
- NP6353.RAbPcr5RtvOvt_qkOEqLM6i0NBgpb-_h9OAzJT3xKO6rQ130_assertion SIO_000772 20818383 NP6353.RAbPcr5RtvOvt_qkOEqLM6i0NBgpb-_h9OAzJT3xKO6rQ130_provenance.
- NP6353.RAbPcr5RtvOvt_qkOEqLM6i0NBgpb-_h9OAzJT3xKO6rQ130_assertion wasDerivedFrom uniprot-2016 NP6353.RAbPcr5RtvOvt_qkOEqLM6i0NBgpb-_h9OAzJT3xKO6rQ130_provenance.
- NP6353.RAbPcr5RtvOvt_qkOEqLM6i0NBgpb-_h9OAzJT3xKO6rQ130_assertion wasGeneratedBy ECO_0000218 NP6353.RAbPcr5RtvOvt_qkOEqLM6i0NBgpb-_h9OAzJT3xKO6rQ130_provenance.