Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP100324.RAtnJH4bDcS5AcjN0ln4MKyHS7Yj0INlg49NxYiVYOYLQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP100324.RAtnJH4bDcS5AcjN0ln4MKyHS7Yj0INlg49NxYiVYOYLQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP100324.RAtnJH4bDcS5AcjN0ln4MKyHS7Yj0INlg49NxYiVYOYLQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP100324.RAtnJH4bDcS5AcjN0ln4MKyHS7Yj0INlg49NxYiVYOYLQ130_provenance.
- NP100324.RAtnJH4bDcS5AcjN0ln4MKyHS7Yj0INlg49NxYiVYOYLQ130_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." NP100324.RAtnJH4bDcS5AcjN0ln4MKyHS7Yj0INlg49NxYiVYOYLQ130_provenance.
- NP100324.RAtnJH4bDcS5AcjN0ln4MKyHS7Yj0INlg49NxYiVYOYLQ130_assertion evidence source_evidence_literature NP100324.RAtnJH4bDcS5AcjN0ln4MKyHS7Yj0INlg49NxYiVYOYLQ130_provenance.
- NP100324.RAtnJH4bDcS5AcjN0ln4MKyHS7Yj0INlg49NxYiVYOYLQ130_assertion SIO_000772 16645216 NP100324.RAtnJH4bDcS5AcjN0ln4MKyHS7Yj0INlg49NxYiVYOYLQ130_provenance.
- NP100324.RAtnJH4bDcS5AcjN0ln4MKyHS7Yj0INlg49NxYiVYOYLQ130_assertion wasDerivedFrom gad-20150221 NP100324.RAtnJH4bDcS5AcjN0ln4MKyHS7Yj0INlg49NxYiVYOYLQ130_provenance.
- NP100324.RAtnJH4bDcS5AcjN0ln4MKyHS7Yj0INlg49NxYiVYOYLQ130_assertion wasGeneratedBy ECO_0000203 NP100324.RAtnJH4bDcS5AcjN0ln4MKyHS7Yj0INlg49NxYiVYOYLQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP100324.RAtnJH4bDcS5AcjN0ln4MKyHS7Yj0INlg49NxYiVYOYLQ130_provenance.