Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP252928.RAdYg-BESm4fqK9jYrxD4o7rXqpWs78l7XrhPnI6BgLaM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP252928.RAdYg-BESm4fqK9jYrxD4o7rXqpWs78l7XrhPnI6BgLaM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP252928.RAdYg-BESm4fqK9jYrxD4o7rXqpWs78l7XrhPnI6BgLaM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP252928.RAdYg-BESm4fqK9jYrxD4o7rXqpWs78l7XrhPnI6BgLaM130_provenance.
- NP252928.RAdYg-BESm4fqK9jYrxD4o7rXqpWs78l7XrhPnI6BgLaM130_assertion description "[Myotonic dystrophy (DM), the most common inherited muscle disorder, is caused by a CTG expansion in the 3-untranslated region of a protein kinase gene ( DMPK ).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP252928.RAdYg-BESm4fqK9jYrxD4o7rXqpWs78l7XrhPnI6BgLaM130_provenance.
- NP252928.RAdYg-BESm4fqK9jYrxD4o7rXqpWs78l7XrhPnI6BgLaM130_assertion evidence source_evidence_literature NP252928.RAdYg-BESm4fqK9jYrxD4o7rXqpWs78l7XrhPnI6BgLaM130_provenance.
- NP252928.RAdYg-BESm4fqK9jYrxD4o7rXqpWs78l7XrhPnI6BgLaM130_assertion SIO_000772 10332033 NP252928.RAdYg-BESm4fqK9jYrxD4o7rXqpWs78l7XrhPnI6BgLaM130_provenance.
- NP252928.RAdYg-BESm4fqK9jYrxD4o7rXqpWs78l7XrhPnI6BgLaM130_assertion wasDerivedFrom befree-2016 NP252928.RAdYg-BESm4fqK9jYrxD4o7rXqpWs78l7XrhPnI6BgLaM130_provenance.
- NP252928.RAdYg-BESm4fqK9jYrxD4o7rXqpWs78l7XrhPnI6BgLaM130_assertion wasGeneratedBy ECO_0000203 NP252928.RAdYg-BESm4fqK9jYrxD4o7rXqpWs78l7XrhPnI6BgLaM130_provenance.
- befree-2016 importedOn "2016-02-19" NP252928.RAdYg-BESm4fqK9jYrxD4o7rXqpWs78l7XrhPnI6BgLaM130_provenance.