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- NP366819.RA_LRPeRYfYInye51XZYaV4eOkqxBfsIrEUnOgHYPxUSU130_assertion type Assertion NP366819.RA_LRPeRYfYInye51XZYaV4eOkqxBfsIrEUnOgHYPxUSU130_head.
- NP366819.RA_LRPeRYfYInye51XZYaV4eOkqxBfsIrEUnOgHYPxUSU130_assertion description "[The LQTS is caused by mutations in genes encoding cardiac ion channels, and mutations in the genes KVLQT1 and SCNA5 have been identified in cases initially diagnosed as SIDS, in addition to several polymorphisms in these 2 genes and in the HERG gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP366819.RA_LRPeRYfYInye51XZYaV4eOkqxBfsIrEUnOgHYPxUSU130_provenance.
- NP366819.RA_LRPeRYfYInye51XZYaV4eOkqxBfsIrEUnOgHYPxUSU130_assertion evidence source_evidence_literature NP366819.RA_LRPeRYfYInye51XZYaV4eOkqxBfsIrEUnOgHYPxUSU130_provenance.
- NP366819.RA_LRPeRYfYInye51XZYaV4eOkqxBfsIrEUnOgHYPxUSU130_assertion SIO_000772 15466077 NP366819.RA_LRPeRYfYInye51XZYaV4eOkqxBfsIrEUnOgHYPxUSU130_provenance.
- NP366819.RA_LRPeRYfYInye51XZYaV4eOkqxBfsIrEUnOgHYPxUSU130_assertion wasDerivedFrom befree-20140225 NP366819.RA_LRPeRYfYInye51XZYaV4eOkqxBfsIrEUnOgHYPxUSU130_provenance.
- NP366819.RA_LRPeRYfYInye51XZYaV4eOkqxBfsIrEUnOgHYPxUSU130_assertion wasGeneratedBy ECO_0000203 NP366819.RA_LRPeRYfYInye51XZYaV4eOkqxBfsIrEUnOgHYPxUSU130_provenance.