Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1216578.RA74xfQPk08L8SOLPFQ6fwEsXfUajvq_895a4XHMWws7k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1216578.RA74xfQPk08L8SOLPFQ6fwEsXfUajvq_895a4XHMWws7k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1216578.RA74xfQPk08L8SOLPFQ6fwEsXfUajvq_895a4XHMWws7k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1216578.RA74xfQPk08L8SOLPFQ6fwEsXfUajvq_895a4XHMWws7k130_provenance.
- NP1216578.RA74xfQPk08L8SOLPFQ6fwEsXfUajvq_895a4XHMWws7k130_assertion description "[Myotonic dystrophy type 2 (DM2) is an autosomal dominant inherited disorder with (CCTG)n repeat expansion in intron 1 of the CNBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216578.RA74xfQPk08L8SOLPFQ6fwEsXfUajvq_895a4XHMWws7k130_provenance.
- NP1216578.RA74xfQPk08L8SOLPFQ6fwEsXfUajvq_895a4XHMWws7k130_assertion evidence source_evidence_literature NP1216578.RA74xfQPk08L8SOLPFQ6fwEsXfUajvq_895a4XHMWws7k130_provenance.
- NP1216578.RA74xfQPk08L8SOLPFQ6fwEsXfUajvq_895a4XHMWws7k130_assertion SIO_000772 25186227 NP1216578.RA74xfQPk08L8SOLPFQ6fwEsXfUajvq_895a4XHMWws7k130_provenance.
- NP1216578.RA74xfQPk08L8SOLPFQ6fwEsXfUajvq_895a4XHMWws7k130_assertion wasDerivedFrom befree-2016 NP1216578.RA74xfQPk08L8SOLPFQ6fwEsXfUajvq_895a4XHMWws7k130_provenance.
- NP1216578.RA74xfQPk08L8SOLPFQ6fwEsXfUajvq_895a4XHMWws7k130_assertion wasGeneratedBy ECO_0000203 NP1216578.RA74xfQPk08L8SOLPFQ6fwEsXfUajvq_895a4XHMWws7k130_provenance.
- befree-2016 importedOn "2016-02-19" NP1216578.RA74xfQPk08L8SOLPFQ6fwEsXfUajvq_895a4XHMWws7k130_provenance.