Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP583478.RA0HTRquLMWqoqPltd7uJH7tcOGrad-8UAVZl1oFWm14s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP583478.RA0HTRquLMWqoqPltd7uJH7tcOGrad-8UAVZl1oFWm14s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583478.RA0HTRquLMWqoqPltd7uJH7tcOGrad-8UAVZl1oFWm14s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583478.RA0HTRquLMWqoqPltd7uJH7tcOGrad-8UAVZl1oFWm14s130_provenance.
- NP583478.RA0HTRquLMWqoqPltd7uJH7tcOGrad-8UAVZl1oFWm14s130_assertion description "[Carnitine-acylcarnitine translocase CACT deficiency is a very rare autosomal recessive disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583478.RA0HTRquLMWqoqPltd7uJH7tcOGrad-8UAVZl1oFWm14s130_provenance.
- NP583478.RA0HTRquLMWqoqPltd7uJH7tcOGrad-8UAVZl1oFWm14s130_assertion evidence source_evidence_literature NP583478.RA0HTRquLMWqoqPltd7uJH7tcOGrad-8UAVZl1oFWm14s130_provenance.
- NP583478.RA0HTRquLMWqoqPltd7uJH7tcOGrad-8UAVZl1oFWm14s130_assertion SIO_000772 15159657 NP583478.RA0HTRquLMWqoqPltd7uJH7tcOGrad-8UAVZl1oFWm14s130_provenance.
- NP583478.RA0HTRquLMWqoqPltd7uJH7tcOGrad-8UAVZl1oFWm14s130_assertion wasDerivedFrom befree-20140225 NP583478.RA0HTRquLMWqoqPltd7uJH7tcOGrad-8UAVZl1oFWm14s130_provenance.
- NP583478.RA0HTRquLMWqoqPltd7uJH7tcOGrad-8UAVZl1oFWm14s130_assertion wasGeneratedBy ECO_0000203 NP583478.RA0HTRquLMWqoqPltd7uJH7tcOGrad-8UAVZl1oFWm14s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP583478.RA0HTRquLMWqoqPltd7uJH7tcOGrad-8UAVZl1oFWm14s130_provenance.