Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP532485.RAJFkd0xceACp39TwVwWyxzSDIxETw4WQdmFbMzp_RbgQ130_assertion> ?p ?o ?g. }
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- NP532485.RAJFkd0xceACp39TwVwWyxzSDIxETw4WQdmFbMzp_RbgQ130_assertion type Assertion NP532485.RAJFkd0xceACp39TwVwWyxzSDIxETw4WQdmFbMzp_RbgQ130_head.
- NP532485.RAJFkd0xceACp39TwVwWyxzSDIxETw4WQdmFbMzp_RbgQ130_assertion description "[This is the first study to identify a dominant mechanism, class 2, for the loss of Kv11.1 channel function in LQT2 and to report that the class 2 phenotype for many of these mutant channels can be corrected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532485.RAJFkd0xceACp39TwVwWyxzSDIxETw4WQdmFbMzp_RbgQ130_provenance.
- NP532485.RAJFkd0xceACp39TwVwWyxzSDIxETw4WQdmFbMzp_RbgQ130_assertion evidence source_evidence_literature NP532485.RAJFkd0xceACp39TwVwWyxzSDIxETw4WQdmFbMzp_RbgQ130_provenance.
- NP532485.RAJFkd0xceACp39TwVwWyxzSDIxETw4WQdmFbMzp_RbgQ130_assertion SIO_000772 16432067 NP532485.RAJFkd0xceACp39TwVwWyxzSDIxETw4WQdmFbMzp_RbgQ130_provenance.
- NP532485.RAJFkd0xceACp39TwVwWyxzSDIxETw4WQdmFbMzp_RbgQ130_assertion wasDerivedFrom befree-2016 NP532485.RAJFkd0xceACp39TwVwWyxzSDIxETw4WQdmFbMzp_RbgQ130_provenance.
- NP532485.RAJFkd0xceACp39TwVwWyxzSDIxETw4WQdmFbMzp_RbgQ130_assertion wasGeneratedBy ECO_0000203 NP532485.RAJFkd0xceACp39TwVwWyxzSDIxETw4WQdmFbMzp_RbgQ130_provenance.