Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP427927.RA5wXHNs_fZP1TNYYD75bLEdX1L2kDEXTc2DBDyOzbSSY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP427927.RA5wXHNs_fZP1TNYYD75bLEdX1L2kDEXTc2DBDyOzbSSY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP427927.RA5wXHNs_fZP1TNYYD75bLEdX1L2kDEXTc2DBDyOzbSSY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP427927.RA5wXHNs_fZP1TNYYD75bLEdX1L2kDEXTc2DBDyOzbSSY130_provenance.
- NP427927.RA5wXHNs_fZP1TNYYD75bLEdX1L2kDEXTc2DBDyOzbSSY130_assertion description "[Myotonic dystrophy (DM) type 1 is caused by an expansion of a CTG repeat in the DMPK gene and type 2 by a CCTG repeat in the ZNF9 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP427927.RA5wXHNs_fZP1TNYYD75bLEdX1L2kDEXTc2DBDyOzbSSY130_provenance.
- NP427927.RA5wXHNs_fZP1TNYYD75bLEdX1L2kDEXTc2DBDyOzbSSY130_assertion evidence source_evidence_literature NP427927.RA5wXHNs_fZP1TNYYD75bLEdX1L2kDEXTc2DBDyOzbSSY130_provenance.
- NP427927.RA5wXHNs_fZP1TNYYD75bLEdX1L2kDEXTc2DBDyOzbSSY130_assertion SIO_000772 14722159 NP427927.RA5wXHNs_fZP1TNYYD75bLEdX1L2kDEXTc2DBDyOzbSSY130_provenance.
- NP427927.RA5wXHNs_fZP1TNYYD75bLEdX1L2kDEXTc2DBDyOzbSSY130_assertion wasDerivedFrom befree-2016 NP427927.RA5wXHNs_fZP1TNYYD75bLEdX1L2kDEXTc2DBDyOzbSSY130_provenance.
- NP427927.RA5wXHNs_fZP1TNYYD75bLEdX1L2kDEXTc2DBDyOzbSSY130_assertion wasGeneratedBy ECO_0000203 NP427927.RA5wXHNs_fZP1TNYYD75bLEdX1L2kDEXTc2DBDyOzbSSY130_provenance.
- befree-2016 importedOn "2016-02-19" NP427927.RA5wXHNs_fZP1TNYYD75bLEdX1L2kDEXTc2DBDyOzbSSY130_provenance.