Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP294370.RAjGPD6nGRdgTDFTfY397TfdywreNARhFV8VTj5GB4Tbg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP294370.RAjGPD6nGRdgTDFTfY397TfdywreNARhFV8VTj5GB4Tbg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294370.RAjGPD6nGRdgTDFTfY397TfdywreNARhFV8VTj5GB4Tbg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294370.RAjGPD6nGRdgTDFTfY397TfdywreNARhFV8VTj5GB4Tbg130_provenance.
- NP294370.RAjGPD6nGRdgTDFTfY397TfdywreNARhFV8VTj5GB4Tbg130_assertion description "[Myotonic dystrophy (DM), the most common form of muscular dystrophy in adult humans, results from expansion of a CTG repeat in the 3' untranslated region of the DMPK gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294370.RAjGPD6nGRdgTDFTfY397TfdywreNARhFV8VTj5GB4Tbg130_provenance.
- NP294370.RAjGPD6nGRdgTDFTfY397TfdywreNARhFV8VTj5GB4Tbg130_assertion evidence source_evidence_literature NP294370.RAjGPD6nGRdgTDFTfY397TfdywreNARhFV8VTj5GB4Tbg130_provenance.
- NP294370.RAjGPD6nGRdgTDFTfY397TfdywreNARhFV8VTj5GB4Tbg130_assertion SIO_000772 10976074 NP294370.RAjGPD6nGRdgTDFTfY397TfdywreNARhFV8VTj5GB4Tbg130_provenance.
- NP294370.RAjGPD6nGRdgTDFTfY397TfdywreNARhFV8VTj5GB4Tbg130_assertion wasDerivedFrom befree-2016 NP294370.RAjGPD6nGRdgTDFTfY397TfdywreNARhFV8VTj5GB4Tbg130_provenance.
- NP294370.RAjGPD6nGRdgTDFTfY397TfdywreNARhFV8VTj5GB4Tbg130_assertion wasGeneratedBy ECO_0000203 NP294370.RAjGPD6nGRdgTDFTfY397TfdywreNARhFV8VTj5GB4Tbg130_provenance.
- befree-2016 importedOn "2016-02-19" NP294370.RAjGPD6nGRdgTDFTfY397TfdywreNARhFV8VTj5GB4Tbg130_provenance.