Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP186606.RAHyGsYHBpu8nVTJMCYdOHhv03J8ayDRY0EDQjxrZo6AQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP186606.RAHyGsYHBpu8nVTJMCYdOHhv03J8ayDRY0EDQjxrZo6AQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP186606.RAHyGsYHBpu8nVTJMCYdOHhv03J8ayDRY0EDQjxrZo6AQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP186606.RAHyGsYHBpu8nVTJMCYdOHhv03J8ayDRY0EDQjxrZo6AQ130_provenance.
- NP186606.RAHyGsYHBpu8nVTJMCYdOHhv03J8ayDRY0EDQjxrZo6AQ130_assertion description "[in a kindred with a syndrome including hypertension, hypercholesterolemia & hypomagnesemia, analysis of maternal lineage mitochondrial genome identified a mutation substituting cytidine for uridine immediately 5'to the mitochondrial TRNA (Ile) anticodon]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186606.RAHyGsYHBpu8nVTJMCYdOHhv03J8ayDRY0EDQjxrZo6AQ130_provenance.
- NP186606.RAHyGsYHBpu8nVTJMCYdOHhv03J8ayDRY0EDQjxrZo6AQ130_assertion evidence source_evidence_literature NP186606.RAHyGsYHBpu8nVTJMCYdOHhv03J8ayDRY0EDQjxrZo6AQ130_provenance.
- NP186606.RAHyGsYHBpu8nVTJMCYdOHhv03J8ayDRY0EDQjxrZo6AQ130_assertion SIO_000772 15498972 NP186606.RAHyGsYHBpu8nVTJMCYdOHhv03J8ayDRY0EDQjxrZo6AQ130_provenance.
- NP186606.RAHyGsYHBpu8nVTJMCYdOHhv03J8ayDRY0EDQjxrZo6AQ130_assertion wasDerivedFrom lhgdn-20090331 NP186606.RAHyGsYHBpu8nVTJMCYdOHhv03J8ayDRY0EDQjxrZo6AQ130_provenance.
- NP186606.RAHyGsYHBpu8nVTJMCYdOHhv03J8ayDRY0EDQjxrZo6AQ130_assertion wasGeneratedBy ECO_0000203 NP186606.RAHyGsYHBpu8nVTJMCYdOHhv03J8ayDRY0EDQjxrZo6AQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP186606.RAHyGsYHBpu8nVTJMCYdOHhv03J8ayDRY0EDQjxrZo6AQ130_provenance.