Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_provenance.
- NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_assertion description "[The mutation causing myotonic dystrophy (DM) has recently been identified as an unstable CTG trinucleotide repeat located in the 3' untranslated region of a gene encoding for a protein with putative serine-threonine protein kinase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_provenance.
- NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_assertion evidence source_evidence_literature NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_provenance.
- NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_assertion SIO_000772 8499920 NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_provenance.
- NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_assertion wasDerivedFrom befree-20140225 NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_provenance.
- NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_assertion wasGeneratedBy ECO_0000203 NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_provenance.