Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP263141.RANQVkPhMsWzUVwNPdW9402GE9H4NXP5_8mKpklqzR0Dk130_assertion> ?p ?o ?g. }
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- NP263141.RANQVkPhMsWzUVwNPdW9402GE9H4NXP5_8mKpklqzR0Dk130_assertion type Assertion NP263141.RANQVkPhMsWzUVwNPdW9402GE9H4NXP5_8mKpklqzR0Dk130_head.
- NP263141.RANQVkPhMsWzUVwNPdW9402GE9H4NXP5_8mKpklqzR0Dk130_assertion description "[KCNQ1 mutations that disrupt this complex cause type 1 long-QT syndrome (LQT1), one of the potentially lethal heritable arrhythmia syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263141.RANQVkPhMsWzUVwNPdW9402GE9H4NXP5_8mKpklqzR0Dk130_provenance.
- NP263141.RANQVkPhMsWzUVwNPdW9402GE9H4NXP5_8mKpklqzR0Dk130_assertion evidence source_evidence_literature NP263141.RANQVkPhMsWzUVwNPdW9402GE9H4NXP5_8mKpklqzR0Dk130_provenance.
- NP263141.RANQVkPhMsWzUVwNPdW9402GE9H4NXP5_8mKpklqzR0Dk130_assertion SIO_000772 18093912 NP263141.RANQVkPhMsWzUVwNPdW9402GE9H4NXP5_8mKpklqzR0Dk130_provenance.
- NP263141.RANQVkPhMsWzUVwNPdW9402GE9H4NXP5_8mKpklqzR0Dk130_assertion wasDerivedFrom befree-20140225 NP263141.RANQVkPhMsWzUVwNPdW9402GE9H4NXP5_8mKpklqzR0Dk130_provenance.
- NP263141.RANQVkPhMsWzUVwNPdW9402GE9H4NXP5_8mKpklqzR0Dk130_assertion wasGeneratedBy ECO_0000203 NP263141.RANQVkPhMsWzUVwNPdW9402GE9H4NXP5_8mKpklqzR0Dk130_provenance.