Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1216578.RA74xfQPk08L8SOLPFQ6fwEsXfUajvq_895a4XHMWws7k130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1216578.RA74xfQPk08L8SOLPFQ6fwEsXfUajvq_895a4XHMWws7k130_assertion type Assertion NP1216578.RA74xfQPk08L8SOLPFQ6fwEsXfUajvq_895a4XHMWws7k130_head.
- 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.