Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP331525.RAbNGwZZtSiDTNlrzeosDs3Kq7FZtLtfyZ4AKjUmk7jKA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP331525.RAbNGwZZtSiDTNlrzeosDs3Kq7FZtLtfyZ4AKjUmk7jKA130_assertion type Assertion NP331525.RAbNGwZZtSiDTNlrzeosDs3Kq7FZtLtfyZ4AKjUmk7jKA130_head.
- NP331525.RAbNGwZZtSiDTNlrzeosDs3Kq7FZtLtfyZ4AKjUmk7jKA130_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." NP331525.RAbNGwZZtSiDTNlrzeosDs3Kq7FZtLtfyZ4AKjUmk7jKA130_provenance.
- NP331525.RAbNGwZZtSiDTNlrzeosDs3Kq7FZtLtfyZ4AKjUmk7jKA130_assertion evidence source_evidence_literature NP331525.RAbNGwZZtSiDTNlrzeosDs3Kq7FZtLtfyZ4AKjUmk7jKA130_provenance.
- NP331525.RAbNGwZZtSiDTNlrzeosDs3Kq7FZtLtfyZ4AKjUmk7jKA130_assertion SIO_000772 16645216 NP331525.RAbNGwZZtSiDTNlrzeosDs3Kq7FZtLtfyZ4AKjUmk7jKA130_provenance.
- NP331525.RAbNGwZZtSiDTNlrzeosDs3Kq7FZtLtfyZ4AKjUmk7jKA130_assertion wasDerivedFrom befree-20140225 NP331525.RAbNGwZZtSiDTNlrzeosDs3Kq7FZtLtfyZ4AKjUmk7jKA130_provenance.
- NP331525.RAbNGwZZtSiDTNlrzeosDs3Kq7FZtLtfyZ4AKjUmk7jKA130_assertion wasGeneratedBy ECO_0000203 NP331525.RAbNGwZZtSiDTNlrzeosDs3Kq7FZtLtfyZ4AKjUmk7jKA130_provenance.