Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP782559.RANX0H1CcwxU5Ryfs3_LjZFB91dDindosnM9yDQXVx5tI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP782559.RANX0H1CcwxU5Ryfs3_LjZFB91dDindosnM9yDQXVx5tI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP782559.RANX0H1CcwxU5Ryfs3_LjZFB91dDindosnM9yDQXVx5tI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP782559.RANX0H1CcwxU5Ryfs3_LjZFB91dDindosnM9yDQXVx5tI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP782559.RANX0H1CcwxU5Ryfs3_LjZFB91dDindosnM9yDQXVx5tI130_provenance.
- 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.