Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1098402.RA3NCAJtg_fJEF5m2MTZf_4Q2WYpq0tUOrVPiz0PMRf_E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1098402.RA3NCAJtg_fJEF5m2MTZf_4Q2WYpq0tUOrVPiz0PMRf_E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1098402.RA3NCAJtg_fJEF5m2MTZf_4Q2WYpq0tUOrVPiz0PMRf_E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1098402.RA3NCAJtg_fJEF5m2MTZf_4Q2WYpq0tUOrVPiz0PMRf_E130_provenance.
- befree-2016 importedOn "2016-02-19" NP1098402.RA3NCAJtg_fJEF5m2MTZf_4Q2WYpq0tUOrVPiz0PMRf_E130_provenance.
- NP1098402.RA3NCAJtg_fJEF5m2MTZf_4Q2WYpq0tUOrVPiz0PMRf_E130_assertion wasGeneratedBy ECO_0000203 NP1098402.RA3NCAJtg_fJEF5m2MTZf_4Q2WYpq0tUOrVPiz0PMRf_E130_provenance.
- NP1098402.RA3NCAJtg_fJEF5m2MTZf_4Q2WYpq0tUOrVPiz0PMRf_E130_assertion wasDerivedFrom befree-2016 NP1098402.RA3NCAJtg_fJEF5m2MTZf_4Q2WYpq0tUOrVPiz0PMRf_E130_provenance.
- NP1098402.RA3NCAJtg_fJEF5m2MTZf_4Q2WYpq0tUOrVPiz0PMRf_E130_assertion SIO_000772 23901116 NP1098402.RA3NCAJtg_fJEF5m2MTZf_4Q2WYpq0tUOrVPiz0PMRf_E130_provenance.
- NP1098402.RA3NCAJtg_fJEF5m2MTZf_4Q2WYpq0tUOrVPiz0PMRf_E130_assertion evidence source_evidence_literature NP1098402.RA3NCAJtg_fJEF5m2MTZf_4Q2WYpq0tUOrVPiz0PMRf_E130_provenance.
- NP1098402.RA3NCAJtg_fJEF5m2MTZf_4Q2WYpq0tUOrVPiz0PMRf_E130_assertion description "[Myotonic dystrophy type 1 (DM1) is caused by expansion of CTG repeats in the 3' UTR of the DMPK gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1098402.RA3NCAJtg_fJEF5m2MTZf_4Q2WYpq0tUOrVPiz0PMRf_E130_provenance.