Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP712756.RADTCeiy1FFAj4_hpTIZVRMDE6slHAaY_8l-w2pLx1pfQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP712756.RADTCeiy1FFAj4_hpTIZVRMDE6slHAaY_8l-w2pLx1pfQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP712756.RADTCeiy1FFAj4_hpTIZVRMDE6slHAaY_8l-w2pLx1pfQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP712756.RADTCeiy1FFAj4_hpTIZVRMDE6slHAaY_8l-w2pLx1pfQ130_provenance.
- NP712756.RADTCeiy1FFAj4_hpTIZVRMDE6slHAaY_8l-w2pLx1pfQ130_assertion description "[Myotonic dystrophy type 1 (DM1) is an autosomal-dominant muscular dystrophy caused by expansion of cytosine-thymine-guanine (CTG) trinucleotide repeats in the myotonic dystrophy protein kinase (DMPK) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP712756.RADTCeiy1FFAj4_hpTIZVRMDE6slHAaY_8l-w2pLx1pfQ130_provenance.
- NP712756.RADTCeiy1FFAj4_hpTIZVRMDE6slHAaY_8l-w2pLx1pfQ130_assertion evidence source_evidence_literature NP712756.RADTCeiy1FFAj4_hpTIZVRMDE6slHAaY_8l-w2pLx1pfQ130_provenance.
- NP712756.RADTCeiy1FFAj4_hpTIZVRMDE6slHAaY_8l-w2pLx1pfQ130_assertion SIO_000772 19127114 NP712756.RADTCeiy1FFAj4_hpTIZVRMDE6slHAaY_8l-w2pLx1pfQ130_provenance.
- NP712756.RADTCeiy1FFAj4_hpTIZVRMDE6slHAaY_8l-w2pLx1pfQ130_assertion wasDerivedFrom befree-2016 NP712756.RADTCeiy1FFAj4_hpTIZVRMDE6slHAaY_8l-w2pLx1pfQ130_provenance.
- NP712756.RADTCeiy1FFAj4_hpTIZVRMDE6slHAaY_8l-w2pLx1pfQ130_assertion wasGeneratedBy ECO_0000203 NP712756.RADTCeiy1FFAj4_hpTIZVRMDE6slHAaY_8l-w2pLx1pfQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP712756.RADTCeiy1FFAj4_hpTIZVRMDE6slHAaY_8l-w2pLx1pfQ130_provenance.