Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP463025.RAgOvtu5ZNjmg1hUS0skJkEvyaOOKLgE5gtw3M8PZbOKs130_assertion> ?p ?o ?g. }
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- NP463025.RAgOvtu5ZNjmg1hUS0skJkEvyaOOKLgE5gtw3M8PZbOKs130_assertion type Assertion NP463025.RAgOvtu5ZNjmg1hUS0skJkEvyaOOKLgE5gtw3M8PZbOKs130_head.
- NP463025.RAgOvtu5ZNjmg1hUS0skJkEvyaOOKLgE5gtw3M8PZbOKs130_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." NP463025.RAgOvtu5ZNjmg1hUS0skJkEvyaOOKLgE5gtw3M8PZbOKs130_provenance.
- NP463025.RAgOvtu5ZNjmg1hUS0skJkEvyaOOKLgE5gtw3M8PZbOKs130_assertion evidence source_evidence_literature NP463025.RAgOvtu5ZNjmg1hUS0skJkEvyaOOKLgE5gtw3M8PZbOKs130_provenance.
- NP463025.RAgOvtu5ZNjmg1hUS0skJkEvyaOOKLgE5gtw3M8PZbOKs130_assertion SIO_000772 15466077 NP463025.RAgOvtu5ZNjmg1hUS0skJkEvyaOOKLgE5gtw3M8PZbOKs130_provenance.
- NP463025.RAgOvtu5ZNjmg1hUS0skJkEvyaOOKLgE5gtw3M8PZbOKs130_assertion wasDerivedFrom befree-2016 NP463025.RAgOvtu5ZNjmg1hUS0skJkEvyaOOKLgE5gtw3M8PZbOKs130_provenance.
- NP463025.RAgOvtu5ZNjmg1hUS0skJkEvyaOOKLgE5gtw3M8PZbOKs130_assertion wasGeneratedBy ECO_0000203 NP463025.RAgOvtu5ZNjmg1hUS0skJkEvyaOOKLgE5gtw3M8PZbOKs130_provenance.