Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP621001.RABix00dGKDEfvGx6ouFOgh2MBU-azZqiFjKg93ibgZ0U130_assertion> ?p ?o ?g. }
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- NP621001.RABix00dGKDEfvGx6ouFOgh2MBU-azZqiFjKg93ibgZ0U130_assertion type Assertion NP621001.RABix00dGKDEfvGx6ouFOgh2MBU-azZqiFjKg93ibgZ0U130_head.
- NP621001.RABix00dGKDEfvGx6ouFOgh2MBU-azZqiFjKg93ibgZ0U130_assertion wasGeneratedBy ECO_0000203 NP621001.RABix00dGKDEfvGx6ouFOgh2MBU-azZqiFjKg93ibgZ0U130_provenance.
- NP621001.RABix00dGKDEfvGx6ouFOgh2MBU-azZqiFjKg93ibgZ0U130_assertion wasDerivedFrom befree-20140225 NP621001.RABix00dGKDEfvGx6ouFOgh2MBU-azZqiFjKg93ibgZ0U130_provenance.
- NP621001.RABix00dGKDEfvGx6ouFOgh2MBU-azZqiFjKg93ibgZ0U130_assertion SIO_000772 17341397 NP621001.RABix00dGKDEfvGx6ouFOgh2MBU-azZqiFjKg93ibgZ0U130_provenance.
- NP621001.RABix00dGKDEfvGx6ouFOgh2MBU-azZqiFjKg93ibgZ0U130_assertion evidence source_evidence_literature NP621001.RABix00dGKDEfvGx6ouFOgh2MBU-azZqiFjKg93ibgZ0U130_provenance.
- NP621001.RABix00dGKDEfvGx6ouFOgh2MBU-azZqiFjKg93ibgZ0U130_assertion description "[Loss-of-function mutations in the KCNJ2 cause approximately 50% of Andersen-Tawil Syndrome (ATS) characterized by a classic triad of periodic paralysis, ventricular arrhythmia, and dysmorphic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621001.RABix00dGKDEfvGx6ouFOgh2MBU-azZqiFjKg93ibgZ0U130_provenance.