Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP739558.RAOgPhee7WSVsvI6fStv8uoghrGU6uOBWwFOnw9FkGIk8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP739558.RAOgPhee7WSVsvI6fStv8uoghrGU6uOBWwFOnw9FkGIk8130_assertion type Assertion NP739558.RAOgPhee7WSVsvI6fStv8uoghrGU6uOBWwFOnw9FkGIk8130_head.
- NP739558.RAOgPhee7WSVsvI6fStv8uoghrGU6uOBWwFOnw9FkGIk8130_assertion description "[Detection of common disease-causing mutations in mitochondrial DNA (mitochondrial encephalomyopathy, lactic acidosis with stroke-like episodes MTTL1 3243 A>G and myoclonic epilepsy associated with ragged-red fibers MTTK 8344A>G) by real-time polymerase chain reaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP739558.RAOgPhee7WSVsvI6fStv8uoghrGU6uOBWwFOnw9FkGIk8130_provenance.
- NP739558.RAOgPhee7WSVsvI6fStv8uoghrGU6uOBWwFOnw9FkGIk8130_assertion evidence source_evidence_literature NP739558.RAOgPhee7WSVsvI6fStv8uoghrGU6uOBWwFOnw9FkGIk8130_provenance.
- NP739558.RAOgPhee7WSVsvI6fStv8uoghrGU6uOBWwFOnw9FkGIk8130_assertion SIO_000772 16645216 NP739558.RAOgPhee7WSVsvI6fStv8uoghrGU6uOBWwFOnw9FkGIk8130_provenance.
- NP739558.RAOgPhee7WSVsvI6fStv8uoghrGU6uOBWwFOnw9FkGIk8130_assertion wasDerivedFrom befree-20150227 NP739558.RAOgPhee7WSVsvI6fStv8uoghrGU6uOBWwFOnw9FkGIk8130_provenance.
- NP739558.RAOgPhee7WSVsvI6fStv8uoghrGU6uOBWwFOnw9FkGIk8130_assertion wasGeneratedBy ECO_0000203 NP739558.RAOgPhee7WSVsvI6fStv8uoghrGU6uOBWwFOnw9FkGIk8130_provenance.