Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP802830.RAzpT49dUyN65JJ6vxD-7qQsFxhdPqKhrzbYSOet7bOJo130_assertion> ?p ?o ?g. }
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- NP802830.RAzpT49dUyN65JJ6vxD-7qQsFxhdPqKhrzbYSOet7bOJo130_assertion type Assertion NP802830.RAzpT49dUyN65JJ6vxD-7qQsFxhdPqKhrzbYSOet7bOJo130_head.
- NP802830.RAzpT49dUyN65JJ6vxD-7qQsFxhdPqKhrzbYSOet7bOJo130_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." NP802830.RAzpT49dUyN65JJ6vxD-7qQsFxhdPqKhrzbYSOet7bOJo130_provenance.
- NP802830.RAzpT49dUyN65JJ6vxD-7qQsFxhdPqKhrzbYSOet7bOJo130_assertion evidence source_evidence_literature NP802830.RAzpT49dUyN65JJ6vxD-7qQsFxhdPqKhrzbYSOet7bOJo130_provenance.
- NP802830.RAzpT49dUyN65JJ6vxD-7qQsFxhdPqKhrzbYSOet7bOJo130_assertion SIO_000772 20346670 NP802830.RAzpT49dUyN65JJ6vxD-7qQsFxhdPqKhrzbYSOet7bOJo130_provenance.
- NP802830.RAzpT49dUyN65JJ6vxD-7qQsFxhdPqKhrzbYSOet7bOJo130_assertion wasDerivedFrom befree-2016 NP802830.RAzpT49dUyN65JJ6vxD-7qQsFxhdPqKhrzbYSOet7bOJo130_provenance.
- NP802830.RAzpT49dUyN65JJ6vxD-7qQsFxhdPqKhrzbYSOet7bOJo130_assertion wasGeneratedBy ECO_0000203 NP802830.RAzpT49dUyN65JJ6vxD-7qQsFxhdPqKhrzbYSOet7bOJo130_provenance.