Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP276024.RAt8YI8HDPaSMboGB6sNNRsZcN2EHnSrJq61Pi1H3NNFg130_assertion> ?p ?o ?g. }
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- NP276024.RAt8YI8HDPaSMboGB6sNNRsZcN2EHnSrJq61Pi1H3NNFg130_assertion type Assertion NP276024.RAt8YI8HDPaSMboGB6sNNRsZcN2EHnSrJq61Pi1H3NNFg130_head.
- NP276024.RAt8YI8HDPaSMboGB6sNNRsZcN2EHnSrJq61Pi1H3NNFg130_assertion description "[Genetic studies have identified four forms of congenital long QT syndrome (LQTS) caused by mutations in ion channel genes located on chromosomes 3 (LQT3), 7 (LQT2), 11 (LQT1), and 21 (LQT5).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276024.RAt8YI8HDPaSMboGB6sNNRsZcN2EHnSrJq61Pi1H3NNFg130_provenance.
- NP276024.RAt8YI8HDPaSMboGB6sNNRsZcN2EHnSrJq61Pi1H3NNFg130_assertion evidence source_evidence_literature NP276024.RAt8YI8HDPaSMboGB6sNNRsZcN2EHnSrJq61Pi1H3NNFg130_provenance.
- NP276024.RAt8YI8HDPaSMboGB6sNNRsZcN2EHnSrJq61Pi1H3NNFg130_assertion SIO_000772 10688323 NP276024.RAt8YI8HDPaSMboGB6sNNRsZcN2EHnSrJq61Pi1H3NNFg130_provenance.
- NP276024.RAt8YI8HDPaSMboGB6sNNRsZcN2EHnSrJq61Pi1H3NNFg130_assertion wasDerivedFrom befree-2016 NP276024.RAt8YI8HDPaSMboGB6sNNRsZcN2EHnSrJq61Pi1H3NNFg130_provenance.
- NP276024.RAt8YI8HDPaSMboGB6sNNRsZcN2EHnSrJq61Pi1H3NNFg130_assertion wasGeneratedBy ECO_0000203 NP276024.RAt8YI8HDPaSMboGB6sNNRsZcN2EHnSrJq61Pi1H3NNFg130_provenance.