Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP608940.RAKStlqUW0or_3uVZKVjIAjSKFIRzfVs11QQvYL5wL-wE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP608940.RAKStlqUW0or_3uVZKVjIAjSKFIRzfVs11QQvYL5wL-wE130_assertion type Assertion NP608940.RAKStlqUW0or_3uVZKVjIAjSKFIRzfVs11QQvYL5wL-wE130_head.
- NP608940.RAKStlqUW0or_3uVZKVjIAjSKFIRzfVs11QQvYL5wL-wE130_assertion wasGeneratedBy ECO_0000203 NP608940.RAKStlqUW0or_3uVZKVjIAjSKFIRzfVs11QQvYL5wL-wE130_provenance.
- NP608940.RAKStlqUW0or_3uVZKVjIAjSKFIRzfVs11QQvYL5wL-wE130_assertion wasDerivedFrom befree-2016 NP608940.RAKStlqUW0or_3uVZKVjIAjSKFIRzfVs11QQvYL5wL-wE130_provenance.
- NP608940.RAKStlqUW0or_3uVZKVjIAjSKFIRzfVs11QQvYL5wL-wE130_assertion SIO_000772 17487865 NP608940.RAKStlqUW0or_3uVZKVjIAjSKFIRzfVs11QQvYL5wL-wE130_provenance.
- NP608940.RAKStlqUW0or_3uVZKVjIAjSKFIRzfVs11QQvYL5wL-wE130_assertion evidence source_evidence_literature NP608940.RAKStlqUW0or_3uVZKVjIAjSKFIRzfVs11QQvYL5wL-wE130_provenance.
- NP608940.RAKStlqUW0or_3uVZKVjIAjSKFIRzfVs11QQvYL5wL-wE130_assertion description "[Myotonic dystrophy type1 (DM1) is a multisystemic disorder caused by a CTG repeat expansion in the DMPK gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP608940.RAKStlqUW0or_3uVZKVjIAjSKFIRzfVs11QQvYL5wL-wE130_provenance.