Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP65470.RAOPS_Zv_lGFE9qwiOWrW2B9I7v4LT8qPGJh9q3bECjaU130_assertion> ?p ?o ?g. }
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- NP65470.RAOPS_Zv_lGFE9qwiOWrW2B9I7v4LT8qPGJh9q3bECjaU130_assertion type Assertion NP65470.RAOPS_Zv_lGFE9qwiOWrW2B9I7v4LT8qPGJh9q3bECjaU130_head.
- NP65470.RAOPS_Zv_lGFE9qwiOWrW2B9I7v4LT8qPGJh9q3bECjaU130_assertion description "[Mutations in the KCNQ1, HERG, SCN5A, minK and MiRP1 genes cause long QT syndrome (LQTS), of which there are two forms: the Romano Ward syndrome and the Jervell and Lange-Nielsen syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65470.RAOPS_Zv_lGFE9qwiOWrW2B9I7v4LT8qPGJh9q3bECjaU130_provenance.
- NP65470.RAOPS_Zv_lGFE9qwiOWrW2B9I7v4LT8qPGJh9q3bECjaU130_assertion evidence source_evidence_literature NP65470.RAOPS_Zv_lGFE9qwiOWrW2B9I7v4LT8qPGJh9q3bECjaU130_provenance.
- NP65470.RAOPS_Zv_lGFE9qwiOWrW2B9I7v4LT8qPGJh9q3bECjaU130_assertion SIO_000772 18752142 NP65470.RAOPS_Zv_lGFE9qwiOWrW2B9I7v4LT8qPGJh9q3bECjaU130_provenance.
- NP65470.RAOPS_Zv_lGFE9qwiOWrW2B9I7v4LT8qPGJh9q3bECjaU130_assertion wasDerivedFrom gad-20130706 NP65470.RAOPS_Zv_lGFE9qwiOWrW2B9I7v4LT8qPGJh9q3bECjaU130_provenance.
- NP65470.RAOPS_Zv_lGFE9qwiOWrW2B9I7v4LT8qPGJh9q3bECjaU130_assertion wasGeneratedBy ECO_0000203 NP65470.RAOPS_Zv_lGFE9qwiOWrW2B9I7v4LT8qPGJh9q3bECjaU130_provenance.