Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP355962.RA0AxQF4swg0yfDC7WCravCczDzdEXAKaX5ncwLhK9Y2I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP355962.RA0AxQF4swg0yfDC7WCravCczDzdEXAKaX5ncwLhK9Y2I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP355962.RA0AxQF4swg0yfDC7WCravCczDzdEXAKaX5ncwLhK9Y2I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP355962.RA0AxQF4swg0yfDC7WCravCczDzdEXAKaX5ncwLhK9Y2I130_provenance.
- NP355962.RA0AxQF4swg0yfDC7WCravCczDzdEXAKaX5ncwLhK9Y2I130_assertion description "[Myotonic dystrophy type 1 (DM1) is a neuromuscular disease caused by the expansion of a CTG repeat in the DMPK gene and characterised by progressive skeletal muscle weakness and wasting.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355962.RA0AxQF4swg0yfDC7WCravCczDzdEXAKaX5ncwLhK9Y2I130_provenance.
- NP355962.RA0AxQF4swg0yfDC7WCravCczDzdEXAKaX5ncwLhK9Y2I130_assertion evidence source_evidence_literature NP355962.RA0AxQF4swg0yfDC7WCravCczDzdEXAKaX5ncwLhK9Y2I130_provenance.
- NP355962.RA0AxQF4swg0yfDC7WCravCczDzdEXAKaX5ncwLhK9Y2I130_assertion SIO_000772 20346670 NP355962.RA0AxQF4swg0yfDC7WCravCczDzdEXAKaX5ncwLhK9Y2I130_provenance.
- NP355962.RA0AxQF4swg0yfDC7WCravCczDzdEXAKaX5ncwLhK9Y2I130_assertion wasDerivedFrom befree-20150227 NP355962.RA0AxQF4swg0yfDC7WCravCczDzdEXAKaX5ncwLhK9Y2I130_provenance.
- NP355962.RA0AxQF4swg0yfDC7WCravCczDzdEXAKaX5ncwLhK9Y2I130_assertion wasGeneratedBy ECO_0000203 NP355962.RA0AxQF4swg0yfDC7WCravCczDzdEXAKaX5ncwLhK9Y2I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP355962.RA0AxQF4swg0yfDC7WCravCczDzdEXAKaX5ncwLhK9Y2I130_provenance.