Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP153539.RAft8Egq37bFVn8TjJxF7DxAedcxXnHbYsM2ryyVCm4zU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP153539.RAft8Egq37bFVn8TjJxF7DxAedcxXnHbYsM2ryyVCm4zU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP153539.RAft8Egq37bFVn8TjJxF7DxAedcxXnHbYsM2ryyVCm4zU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP153539.RAft8Egq37bFVn8TjJxF7DxAedcxXnHbYsM2ryyVCm4zU130_provenance.
- NP153539.RAft8Egq37bFVn8TjJxF7DxAedcxXnHbYsM2ryyVCm4zU130_assertion description "[The results indicate that ACTC1 mutations or reduced ACTC1 levels may lead to atrial septal defect without signs of cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP153539.RAft8Egq37bFVn8TjJxF7DxAedcxXnHbYsM2ryyVCm4zU130_provenance.
- NP153539.RAft8Egq37bFVn8TjJxF7DxAedcxXnHbYsM2ryyVCm4zU130_assertion evidence source_evidence_literature NP153539.RAft8Egq37bFVn8TjJxF7DxAedcxXnHbYsM2ryyVCm4zU130_provenance.
- NP153539.RAft8Egq37bFVn8TjJxF7DxAedcxXnHbYsM2ryyVCm4zU130_assertion SIO_000772 17947298 NP153539.RAft8Egq37bFVn8TjJxF7DxAedcxXnHbYsM2ryyVCm4zU130_provenance.
- NP153539.RAft8Egq37bFVn8TjJxF7DxAedcxXnHbYsM2ryyVCm4zU130_assertion wasDerivedFrom lhgdn-20090331 NP153539.RAft8Egq37bFVn8TjJxF7DxAedcxXnHbYsM2ryyVCm4zU130_provenance.
- NP153539.RAft8Egq37bFVn8TjJxF7DxAedcxXnHbYsM2ryyVCm4zU130_assertion wasGeneratedBy ECO_0000203 NP153539.RAft8Egq37bFVn8TjJxF7DxAedcxXnHbYsM2ryyVCm4zU130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP153539.RAft8Egq37bFVn8TjJxF7DxAedcxXnHbYsM2ryyVCm4zU130_provenance.