Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP4970.RArva80HOCFzAt5EsdaM0LZhfVaM2qjzsG4vwiZtz8vbE130_assertion> ?p ?o ?g. }
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- NP4970.RArva80HOCFzAt5EsdaM0LZhfVaM2qjzsG4vwiZtz8vbE130_assertion type Assertion NP4970.RArva80HOCFzAt5EsdaM0LZhfVaM2qjzsG4vwiZtz8vbE130_head.
- NP4970.RArva80HOCFzAt5EsdaM0LZhfVaM2qjzsG4vwiZtz8vbE130_assertion wasGeneratedBy ECO_0000218 NP4970.RArva80HOCFzAt5EsdaM0LZhfVaM2qjzsG4vwiZtz8vbE130_provenance.
- NP4970.RArva80HOCFzAt5EsdaM0LZhfVaM2qjzsG4vwiZtz8vbE130_assertion wasDerivedFrom uniprot-2016 NP4970.RArva80HOCFzAt5EsdaM0LZhfVaM2qjzsG4vwiZtz8vbE130_provenance.
- NP4970.RArva80HOCFzAt5EsdaM0LZhfVaM2qjzsG4vwiZtz8vbE130_assertion SIO_000772 17458872 NP4970.RArva80HOCFzAt5EsdaM0LZhfVaM2qjzsG4vwiZtz8vbE130_provenance.
- NP4970.RArva80HOCFzAt5EsdaM0LZhfVaM2qjzsG4vwiZtz8vbE130_assertion evidence source_evidence_curated NP4970.RArva80HOCFzAt5EsdaM0LZhfVaM2qjzsG4vwiZtz8vbE130_provenance.
- NP4970.RArva80HOCFzAt5EsdaM0LZhfVaM2qjzsG4vwiZtz8vbE130_assertion description "[These results explain why this patient with a mutation in exon 3II of the ACOX1 gene, but with normal expression of exon 3I, was indistinguishable from other patients with peroxisomal acyl-CoA oxidase deficiency with respect to his clinical presentation and the biochemical abnormalities in his fibroblasts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4970.RArva80HOCFzAt5EsdaM0LZhfVaM2qjzsG4vwiZtz8vbE130_provenance.