Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP783217.RAV1wFswLoehWsxPJbIsy5_Pp4IxTsXVRtqwdYZYvEsEs130_assertion> ?p ?o ?g. }
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- NP783217.RAV1wFswLoehWsxPJbIsy5_Pp4IxTsXVRtqwdYZYvEsEs130_assertion type Assertion NP783217.RAV1wFswLoehWsxPJbIsy5_Pp4IxTsXVRtqwdYZYvEsEs130_head.
- NP783217.RAV1wFswLoehWsxPJbIsy5_Pp4IxTsXVRtqwdYZYvEsEs130_assertion description "[Andersen-Tawil syndrome, a skeletal muscle syndrome associated with periodic paralysis and long QT intervals on the ECG, has been linked to defects in KCNJ2, the gene encoding for the inward rectifier potassium channel (I(K1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783217.RAV1wFswLoehWsxPJbIsy5_Pp4IxTsXVRtqwdYZYvEsEs130_provenance.
- NP783217.RAV1wFswLoehWsxPJbIsy5_Pp4IxTsXVRtqwdYZYvEsEs130_assertion evidence source_evidence_literature NP783217.RAV1wFswLoehWsxPJbIsy5_Pp4IxTsXVRtqwdYZYvEsEs130_provenance.
- NP783217.RAV1wFswLoehWsxPJbIsy5_Pp4IxTsXVRtqwdYZYvEsEs130_assertion SIO_000772 16500306 NP783217.RAV1wFswLoehWsxPJbIsy5_Pp4IxTsXVRtqwdYZYvEsEs130_provenance.
- NP783217.RAV1wFswLoehWsxPJbIsy5_Pp4IxTsXVRtqwdYZYvEsEs130_assertion wasDerivedFrom befree-20140225 NP783217.RAV1wFswLoehWsxPJbIsy5_Pp4IxTsXVRtqwdYZYvEsEs130_provenance.
- NP783217.RAV1wFswLoehWsxPJbIsy5_Pp4IxTsXVRtqwdYZYvEsEs130_assertion wasGeneratedBy ECO_0000203 NP783217.RAV1wFswLoehWsxPJbIsy5_Pp4IxTsXVRtqwdYZYvEsEs130_provenance.