Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP443191.RAV_EsF6xrvAE1hTfb7C5WXZpBhvYZz6piuqCYCUfgDcQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP443191.RAV_EsF6xrvAE1hTfb7C5WXZpBhvYZz6piuqCYCUfgDcQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP443191.RAV_EsF6xrvAE1hTfb7C5WXZpBhvYZz6piuqCYCUfgDcQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP443191.RAV_EsF6xrvAE1hTfb7C5WXZpBhvYZz6piuqCYCUfgDcQ130_provenance.
- NP443191.RAV_EsF6xrvAE1hTfb7C5WXZpBhvYZz6piuqCYCUfgDcQ130_assertion description "[The differentiation of carnitine-acylcarnitine translocase deficiency (CACT) from carnitine palmitoyltransferase type II deficiency (CPT-II) and long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency from mitochondrial trifunctional protein deficiency (MTP) continues to be ambiguous using current acylcarnitine profiling techniques either from plasma or blood spots, or in the intact cell system (fibroblasts/amniocytes).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP443191.RAV_EsF6xrvAE1hTfb7C5WXZpBhvYZz6piuqCYCUfgDcQ130_provenance.
- NP443191.RAV_EsF6xrvAE1hTfb7C5WXZpBhvYZz6piuqCYCUfgDcQ130_assertion evidence source_evidence_literature NP443191.RAV_EsF6xrvAE1hTfb7C5WXZpBhvYZz6piuqCYCUfgDcQ130_provenance.
- NP443191.RAV_EsF6xrvAE1hTfb7C5WXZpBhvYZz6piuqCYCUfgDcQ130_assertion SIO_000772 16297647 NP443191.RAV_EsF6xrvAE1hTfb7C5WXZpBhvYZz6piuqCYCUfgDcQ130_provenance.
- NP443191.RAV_EsF6xrvAE1hTfb7C5WXZpBhvYZz6piuqCYCUfgDcQ130_assertion wasDerivedFrom befree-20150227 NP443191.RAV_EsF6xrvAE1hTfb7C5WXZpBhvYZz6piuqCYCUfgDcQ130_provenance.
- NP443191.RAV_EsF6xrvAE1hTfb7C5WXZpBhvYZz6piuqCYCUfgDcQ130_assertion wasGeneratedBy ECO_0000203 NP443191.RAV_EsF6xrvAE1hTfb7C5WXZpBhvYZz6piuqCYCUfgDcQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP443191.RAV_EsF6xrvAE1hTfb7C5WXZpBhvYZz6piuqCYCUfgDcQ130_provenance.