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- NP885701.RAWTQYcDO7ljGzuIFIjhzu6xT8o0gwQL5Rlt42vnF4JzY130_assertion type Assertion NP885701.RAWTQYcDO7ljGzuIFIjhzu6xT8o0gwQL5Rlt42vnF4JzY130_head.
- NP885701.RAWTQYcDO7ljGzuIFIjhzu6xT8o0gwQL5Rlt42vnF4JzY130_assertion description "[Genetic analyses revealed that recurrent TdP occurred via electrolyte disturbance and cardiac failure due to PPCM on the basis of a novel mutation in KCNH2, a gene responsible for inherited type 2 long QT syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP885701.RAWTQYcDO7ljGzuIFIjhzu6xT8o0gwQL5Rlt42vnF4JzY130_provenance.
- NP885701.RAWTQYcDO7ljGzuIFIjhzu6xT8o0gwQL5Rlt42vnF4JzY130_assertion evidence source_evidence_literature NP885701.RAWTQYcDO7ljGzuIFIjhzu6xT8o0gwQL5Rlt42vnF4JzY130_provenance.
- NP885701.RAWTQYcDO7ljGzuIFIjhzu6xT8o0gwQL5Rlt42vnF4JzY130_assertion SIO_000772 22382559 NP885701.RAWTQYcDO7ljGzuIFIjhzu6xT8o0gwQL5Rlt42vnF4JzY130_provenance.
- NP885701.RAWTQYcDO7ljGzuIFIjhzu6xT8o0gwQL5Rlt42vnF4JzY130_assertion wasDerivedFrom befree-20140225 NP885701.RAWTQYcDO7ljGzuIFIjhzu6xT8o0gwQL5Rlt42vnF4JzY130_provenance.
- NP885701.RAWTQYcDO7ljGzuIFIjhzu6xT8o0gwQL5Rlt42vnF4JzY130_assertion wasGeneratedBy ECO_0000203 NP885701.RAWTQYcDO7ljGzuIFIjhzu6xT8o0gwQL5Rlt42vnF4JzY130_provenance.