Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[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."@en ?g. }

• 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." provenance.
• NP140.RAPA-mwmRkTghMRpT3cGALss2zoNa4C8w68KjPIMFZjlo130_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." NP140.RAPA-mwmRkTghMRpT3cGALss2zoNa4C8w68KjPIMFZjlo130_provenance.
• NP721864.RAVvv-VYNUQZc_0Pc6aCWO94edlLhchH9aVjtI_Twy1Qw130_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." NP721864.RAVvv-VYNUQZc_0Pc6aCWO94edlLhchH9aVjtI_Twy1Qw130_provenance.
• NP3638.RAhkpJVVLAATiNy7YrVEBzScbNQXCjRVGqAPO--Akkh3k130_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." NP3638.RAhkpJVVLAATiNy7YrVEBzScbNQXCjRVGqAPO--Akkh3k130_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.