Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP583478.RA0HTRquLMWqoqPltd7uJH7tcOGrad-8UAVZl1oFWm14s130_assertion> ?p ?o ?g. }
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- NP583478.RA0HTRquLMWqoqPltd7uJH7tcOGrad-8UAVZl1oFWm14s130_assertion type Assertion NP583478.RA0HTRquLMWqoqPltd7uJH7tcOGrad-8UAVZl1oFWm14s130_head.
- 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.