Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP443196.RAuDbKHcfrsQQs3KjKm8oKZpBAwgY5VRJaVeWnjqq28PA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP443196.RAuDbKHcfrsQQs3KjKm8oKZpBAwgY5VRJaVeWnjqq28PA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP443196.RAuDbKHcfrsQQs3KjKm8oKZpBAwgY5VRJaVeWnjqq28PA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP443196.RAuDbKHcfrsQQs3KjKm8oKZpBAwgY5VRJaVeWnjqq28PA130_provenance.
- NP443196.RAuDbKHcfrsQQs3KjKm8oKZpBAwgY5VRJaVeWnjqq28PA130_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." NP443196.RAuDbKHcfrsQQs3KjKm8oKZpBAwgY5VRJaVeWnjqq28PA130_provenance.
- NP443196.RAuDbKHcfrsQQs3KjKm8oKZpBAwgY5VRJaVeWnjqq28PA130_assertion evidence source_evidence_literature NP443196.RAuDbKHcfrsQQs3KjKm8oKZpBAwgY5VRJaVeWnjqq28PA130_provenance.
- NP443196.RAuDbKHcfrsQQs3KjKm8oKZpBAwgY5VRJaVeWnjqq28PA130_assertion SIO_000772 16297647 NP443196.RAuDbKHcfrsQQs3KjKm8oKZpBAwgY5VRJaVeWnjqq28PA130_provenance.
- NP443196.RAuDbKHcfrsQQs3KjKm8oKZpBAwgY5VRJaVeWnjqq28PA130_assertion wasDerivedFrom befree-20150227 NP443196.RAuDbKHcfrsQQs3KjKm8oKZpBAwgY5VRJaVeWnjqq28PA130_provenance.
- NP443196.RAuDbKHcfrsQQs3KjKm8oKZpBAwgY5VRJaVeWnjqq28PA130_assertion wasGeneratedBy ECO_0000203 NP443196.RAuDbKHcfrsQQs3KjKm8oKZpBAwgY5VRJaVeWnjqq28PA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP443196.RAuDbKHcfrsQQs3KjKm8oKZpBAwgY5VRJaVeWnjqq28PA130_provenance.