Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP782559.RANX0H1CcwxU5Ryfs3_LjZFB91dDindosnM9yDQXVx5tI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP782559.RANX0H1CcwxU5Ryfs3_LjZFB91dDindosnM9yDQXVx5tI130_assertion type Assertion NP782559.RANX0H1CcwxU5Ryfs3_LjZFB91dDindosnM9yDQXVx5tI130_head.
- NP782559.RANX0H1CcwxU5Ryfs3_LjZFB91dDindosnM9yDQXVx5tI130_assertion wasGeneratedBy ECO_0000203 NP782559.RANX0H1CcwxU5Ryfs3_LjZFB91dDindosnM9yDQXVx5tI130_provenance.
- NP782559.RANX0H1CcwxU5Ryfs3_LjZFB91dDindosnM9yDQXVx5tI130_assertion wasDerivedFrom befree-20150227 NP782559.RANX0H1CcwxU5Ryfs3_LjZFB91dDindosnM9yDQXVx5tI130_provenance.
- NP782559.RANX0H1CcwxU5Ryfs3_LjZFB91dDindosnM9yDQXVx5tI130_assertion SIO_000772 22407275 NP782559.RANX0H1CcwxU5Ryfs3_LjZFB91dDindosnM9yDQXVx5tI130_provenance.
- NP782559.RANX0H1CcwxU5Ryfs3_LjZFB91dDindosnM9yDQXVx5tI130_assertion evidence source_evidence_literature NP782559.RANX0H1CcwxU5Ryfs3_LjZFB91dDindosnM9yDQXVx5tI130_provenance.
- NP782559.RANX0H1CcwxU5Ryfs3_LjZFB91dDindosnM9yDQXVx5tI130_assertion description "[Myotonic dystrophy type 2 (DM2) is a common adult onset muscular dystrophy caused by a dominantly transmitted (CCTG)( n ) expansion in intron 1 of the CNBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782559.RANX0H1CcwxU5Ryfs3_LjZFB91dDindosnM9yDQXVx5tI130_provenance.