Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP862559.RANL9ALr9Z1DP_Fb54Qx7nDYTxRFY58DagruRZwu7MPqE130_assertion> ?p ?o ?g. }
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- NP862559.RANL9ALr9Z1DP_Fb54Qx7nDYTxRFY58DagruRZwu7MPqE130_assertion type Assertion NP862559.RANL9ALr9Z1DP_Fb54Qx7nDYTxRFY58DagruRZwu7MPqE130_head.
- NP862559.RANL9ALr9Z1DP_Fb54Qx7nDYTxRFY58DagruRZwu7MPqE130_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." NP862559.RANL9ALr9Z1DP_Fb54Qx7nDYTxRFY58DagruRZwu7MPqE130_provenance.
- NP862559.RANL9ALr9Z1DP_Fb54Qx7nDYTxRFY58DagruRZwu7MPqE130_assertion evidence source_evidence_literature NP862559.RANL9ALr9Z1DP_Fb54Qx7nDYTxRFY58DagruRZwu7MPqE130_provenance.
- NP862559.RANL9ALr9Z1DP_Fb54Qx7nDYTxRFY58DagruRZwu7MPqE130_assertion SIO_000772 18752142 NP862559.RANL9ALr9Z1DP_Fb54Qx7nDYTxRFY58DagruRZwu7MPqE130_provenance.
- NP862559.RANL9ALr9Z1DP_Fb54Qx7nDYTxRFY58DagruRZwu7MPqE130_assertion wasDerivedFrom befree-20140225 NP862559.RANL9ALr9Z1DP_Fb54Qx7nDYTxRFY58DagruRZwu7MPqE130_provenance.
- NP862559.RANL9ALr9Z1DP_Fb54Qx7nDYTxRFY58DagruRZwu7MPqE130_assertion wasGeneratedBy ECO_0000203 NP862559.RANL9ALr9Z1DP_Fb54Qx7nDYTxRFY58DagruRZwu7MPqE130_provenance.