Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP523224.RADelpEkEWIJYTt4FT4f48ZJYthv-N-hwOvVV0gPKX_Es130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP523224.RADelpEkEWIJYTt4FT4f48ZJYthv-N-hwOvVV0gPKX_Es130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP523224.RADelpEkEWIJYTt4FT4f48ZJYthv-N-hwOvVV0gPKX_Es130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP523224.RADelpEkEWIJYTt4FT4f48ZJYthv-N-hwOvVV0gPKX_Es130_provenance.
- NP523224.RADelpEkEWIJYTt4FT4f48ZJYthv-N-hwOvVV0gPKX_Es130_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." NP523224.RADelpEkEWIJYTt4FT4f48ZJYthv-N-hwOvVV0gPKX_Es130_provenance.
- NP523224.RADelpEkEWIJYTt4FT4f48ZJYthv-N-hwOvVV0gPKX_Es130_assertion evidence source_evidence_literature NP523224.RADelpEkEWIJYTt4FT4f48ZJYthv-N-hwOvVV0gPKX_Es130_provenance.
- NP523224.RADelpEkEWIJYTt4FT4f48ZJYthv-N-hwOvVV0gPKX_Es130_assertion SIO_000772 16297647 NP523224.RADelpEkEWIJYTt4FT4f48ZJYthv-N-hwOvVV0gPKX_Es130_provenance.
- NP523224.RADelpEkEWIJYTt4FT4f48ZJYthv-N-hwOvVV0gPKX_Es130_assertion wasDerivedFrom befree-2016 NP523224.RADelpEkEWIJYTt4FT4f48ZJYthv-N-hwOvVV0gPKX_Es130_provenance.
- NP523224.RADelpEkEWIJYTt4FT4f48ZJYthv-N-hwOvVV0gPKX_Es130_assertion wasGeneratedBy ECO_0000203 NP523224.RADelpEkEWIJYTt4FT4f48ZJYthv-N-hwOvVV0gPKX_Es130_provenance.
- befree-2016 importedOn "2016-02-19" NP523224.RADelpEkEWIJYTt4FT4f48ZJYthv-N-hwOvVV0gPKX_Es130_provenance.