Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP227973.RAlViWD863t9aNSaxBYoPix2c42MttsCSlaHRuH0f2uSg130_assertion> ?p ?o ?g. }
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- NP227973.RAlViWD863t9aNSaxBYoPix2c42MttsCSlaHRuH0f2uSg130_assertion type Assertion NP227973.RAlViWD863t9aNSaxBYoPix2c42MttsCSlaHRuH0f2uSg130_head.
- NP227973.RAlViWD863t9aNSaxBYoPix2c42MttsCSlaHRuH0f2uSg130_assertion wasGeneratedBy ECO_0000203 NP227973.RAlViWD863t9aNSaxBYoPix2c42MttsCSlaHRuH0f2uSg130_provenance.
- NP227973.RAlViWD863t9aNSaxBYoPix2c42MttsCSlaHRuH0f2uSg130_assertion wasDerivedFrom befree-20140225 NP227973.RAlViWD863t9aNSaxBYoPix2c42MttsCSlaHRuH0f2uSg130_provenance.
- NP227973.RAlViWD863t9aNSaxBYoPix2c42MttsCSlaHRuH0f2uSg130_assertion SIO_000772 18052691 NP227973.RAlViWD863t9aNSaxBYoPix2c42MttsCSlaHRuH0f2uSg130_provenance.
- NP227973.RAlViWD863t9aNSaxBYoPix2c42MttsCSlaHRuH0f2uSg130_assertion evidence source_evidence_literature NP227973.RAlViWD863t9aNSaxBYoPix2c42MttsCSlaHRuH0f2uSg130_provenance.
- NP227973.RAlViWD863t9aNSaxBYoPix2c42MttsCSlaHRuH0f2uSg130_assertion description "[In general, mutations in cardiac ion channel genes (KCNQ1, KCNH2, SCN5A, KCNE1, KCNE2) have been identified as a cause for LQTS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP227973.RAlViWD863t9aNSaxBYoPix2c42MttsCSlaHRuH0f2uSg130_provenance.