Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP134491.RAZtrHcpCaeXnNGFb35rANHZ7btKgRknlz_b0rUTc8kFk130_assertion> ?p ?o ?g. }
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- NP134491.RAZtrHcpCaeXnNGFb35rANHZ7btKgRknlz_b0rUTc8kFk130_assertion type Assertion NP134491.RAZtrHcpCaeXnNGFb35rANHZ7btKgRknlz_b0rUTc8kFk130_head.
- NP134491.RAZtrHcpCaeXnNGFb35rANHZ7btKgRknlz_b0rUTc8kFk130_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." NP134491.RAZtrHcpCaeXnNGFb35rANHZ7btKgRknlz_b0rUTc8kFk130_provenance.
- NP134491.RAZtrHcpCaeXnNGFb35rANHZ7btKgRknlz_b0rUTc8kFk130_assertion evidence source_evidence_literature NP134491.RAZtrHcpCaeXnNGFb35rANHZ7btKgRknlz_b0rUTc8kFk130_provenance.
- NP134491.RAZtrHcpCaeXnNGFb35rANHZ7btKgRknlz_b0rUTc8kFk130_assertion SIO_000772 16645216 NP134491.RAZtrHcpCaeXnNGFb35rANHZ7btKgRknlz_b0rUTc8kFk130_provenance.
- NP134491.RAZtrHcpCaeXnNGFb35rANHZ7btKgRknlz_b0rUTc8kFk130_assertion wasDerivedFrom gad-20150221 NP134491.RAZtrHcpCaeXnNGFb35rANHZ7btKgRknlz_b0rUTc8kFk130_provenance.
- NP134491.RAZtrHcpCaeXnNGFb35rANHZ7btKgRknlz_b0rUTc8kFk130_assertion wasGeneratedBy ECO_0000203 NP134491.RAZtrHcpCaeXnNGFb35rANHZ7btKgRknlz_b0rUTc8kFk130_provenance.