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- source_evidence_literature type ECO_0000212 NP425166.RAroaZ2IA1-xQxjj_AcG6FASWLo9QeAm4NTOjRbnWAfl8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP425166.RAroaZ2IA1-xQxjj_AcG6FASWLo9QeAm4NTOjRbnWAfl8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP425166.RAroaZ2IA1-xQxjj_AcG6FASWLo9QeAm4NTOjRbnWAfl8130_provenance.
- NP425166.RAroaZ2IA1-xQxjj_AcG6FASWLo9QeAm4NTOjRbnWAfl8130_assertion description "[Myotonic dystrophy type 1 (DM1) and type 2 (DM2) are caused by genomic expansions of CTG or CCTG repeats.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP425166.RAroaZ2IA1-xQxjj_AcG6FASWLo9QeAm4NTOjRbnWAfl8130_provenance.
- NP425166.RAroaZ2IA1-xQxjj_AcG6FASWLo9QeAm4NTOjRbnWAfl8130_assertion evidence source_evidence_literature NP425166.RAroaZ2IA1-xQxjj_AcG6FASWLo9QeAm4NTOjRbnWAfl8130_provenance.
- NP425166.RAroaZ2IA1-xQxjj_AcG6FASWLo9QeAm4NTOjRbnWAfl8130_assertion SIO_000772 14681885 NP425166.RAroaZ2IA1-xQxjj_AcG6FASWLo9QeAm4NTOjRbnWAfl8130_provenance.
- NP425166.RAroaZ2IA1-xQxjj_AcG6FASWLo9QeAm4NTOjRbnWAfl8130_assertion wasDerivedFrom befree-2016 NP425166.RAroaZ2IA1-xQxjj_AcG6FASWLo9QeAm4NTOjRbnWAfl8130_provenance.
- NP425166.RAroaZ2IA1-xQxjj_AcG6FASWLo9QeAm4NTOjRbnWAfl8130_assertion wasGeneratedBy ECO_0000203 NP425166.RAroaZ2IA1-xQxjj_AcG6FASWLo9QeAm4NTOjRbnWAfl8130_provenance.
- befree-2016 importedOn "2016-02-19" NP425166.RAroaZ2IA1-xQxjj_AcG6FASWLo9QeAm4NTOjRbnWAfl8130_provenance.