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- source_evidence_literature type ECO_0000212 NP891306.RA-AGNxTwGl3OHo2lYsIvyWw2wpF48e02yVBvUTspLIME130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP891306.RA-AGNxTwGl3OHo2lYsIvyWw2wpF48e02yVBvUTspLIME130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP891306.RA-AGNxTwGl3OHo2lYsIvyWw2wpF48e02yVBvUTspLIME130_provenance.
- NP891306.RA-AGNxTwGl3OHo2lYsIvyWw2wpF48e02yVBvUTspLIME130_assertion description "[Genetic studies excluded mutations in the DM type 1 (DM1) gene, but revealed a CCTG repeat expansion in the ZNF9 gene, which is associated with DM2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP891306.RA-AGNxTwGl3OHo2lYsIvyWw2wpF48e02yVBvUTspLIME130_provenance.
- NP891306.RA-AGNxTwGl3OHo2lYsIvyWw2wpF48e02yVBvUTspLIME130_assertion evidence source_evidence_literature NP891306.RA-AGNxTwGl3OHo2lYsIvyWw2wpF48e02yVBvUTspLIME130_provenance.
- NP891306.RA-AGNxTwGl3OHo2lYsIvyWw2wpF48e02yVBvUTspLIME130_assertion SIO_000772 15704146 NP891306.RA-AGNxTwGl3OHo2lYsIvyWw2wpF48e02yVBvUTspLIME130_provenance.
- NP891306.RA-AGNxTwGl3OHo2lYsIvyWw2wpF48e02yVBvUTspLIME130_assertion wasDerivedFrom befree-20150227 NP891306.RA-AGNxTwGl3OHo2lYsIvyWw2wpF48e02yVBvUTspLIME130_provenance.
- NP891306.RA-AGNxTwGl3OHo2lYsIvyWw2wpF48e02yVBvUTspLIME130_assertion wasGeneratedBy ECO_0000203 NP891306.RA-AGNxTwGl3OHo2lYsIvyWw2wpF48e02yVBvUTspLIME130_provenance.
- befree-20150227 importedOn "2015-02-27" NP891306.RA-AGNxTwGl3OHo2lYsIvyWw2wpF48e02yVBvUTspLIME130_provenance.