Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP802833.RA9jb9AulkfIPWTjkE021FIqp3UZV0-5Hh2soLlOolr2M130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP802833.RA9jb9AulkfIPWTjkE021FIqp3UZV0-5Hh2soLlOolr2M130_assertion type Assertion NP802833.RA9jb9AulkfIPWTjkE021FIqp3UZV0-5Hh2soLlOolr2M130_head.
- NP802833.RA9jb9AulkfIPWTjkE021FIqp3UZV0-5Hh2soLlOolr2M130_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." NP802833.RA9jb9AulkfIPWTjkE021FIqp3UZV0-5Hh2soLlOolr2M130_provenance.
- NP802833.RA9jb9AulkfIPWTjkE021FIqp3UZV0-5Hh2soLlOolr2M130_assertion evidence source_evidence_literature NP802833.RA9jb9AulkfIPWTjkE021FIqp3UZV0-5Hh2soLlOolr2M130_provenance.
- NP802833.RA9jb9AulkfIPWTjkE021FIqp3UZV0-5Hh2soLlOolr2M130_assertion SIO_000772 20346670 NP802833.RA9jb9AulkfIPWTjkE021FIqp3UZV0-5Hh2soLlOolr2M130_provenance.
- NP802833.RA9jb9AulkfIPWTjkE021FIqp3UZV0-5Hh2soLlOolr2M130_assertion wasDerivedFrom befree-2016 NP802833.RA9jb9AulkfIPWTjkE021FIqp3UZV0-5Hh2soLlOolr2M130_provenance.
- NP802833.RA9jb9AulkfIPWTjkE021FIqp3UZV0-5Hh2soLlOolr2M130_assertion wasGeneratedBy ECO_0000203 NP802833.RA9jb9AulkfIPWTjkE021FIqp3UZV0-5Hh2soLlOolr2M130_provenance.