Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP799830.RA7iaoGmMPy0q3rML-Yuhq1SQmc-fFzYq9n__UV6LXPe8130_assertion> ?p ?o ?g. }
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- NP799830.RA7iaoGmMPy0q3rML-Yuhq1SQmc-fFzYq9n__UV6LXPe8130_assertion type Assertion NP799830.RA7iaoGmMPy0q3rML-Yuhq1SQmc-fFzYq9n__UV6LXPe8130_head.
- NP799830.RA7iaoGmMPy0q3rML-Yuhq1SQmc-fFzYq9n__UV6LXPe8130_assertion description "[The periodic paralyses are a group of autosomal dominant muscle diseases sharing the common feature of episodic stiffness and weakness, usually occurring with muscle cooling (as in the case of paramyotonia congenita, PC phenotype) or changes in extracellular K+ levels resulting from various precipitating factors (hyperkalemic periodic paralysis, HYPP and hypokalemic periodic paralysis, HypoPP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP799830.RA7iaoGmMPy0q3rML-Yuhq1SQmc-fFzYq9n__UV6LXPe8130_provenance.
- NP799830.RA7iaoGmMPy0q3rML-Yuhq1SQmc-fFzYq9n__UV6LXPe8130_assertion evidence source_evidence_literature NP799830.RA7iaoGmMPy0q3rML-Yuhq1SQmc-fFzYq9n__UV6LXPe8130_provenance.
- NP799830.RA7iaoGmMPy0q3rML-Yuhq1SQmc-fFzYq9n__UV6LXPe8130_assertion SIO_000772 7721550 NP799830.RA7iaoGmMPy0q3rML-Yuhq1SQmc-fFzYq9n__UV6LXPe8130_provenance.
- NP799830.RA7iaoGmMPy0q3rML-Yuhq1SQmc-fFzYq9n__UV6LXPe8130_assertion wasDerivedFrom befree-20140225 NP799830.RA7iaoGmMPy0q3rML-Yuhq1SQmc-fFzYq9n__UV6LXPe8130_provenance.
- NP799830.RA7iaoGmMPy0q3rML-Yuhq1SQmc-fFzYq9n__UV6LXPe8130_assertion wasGeneratedBy ECO_0000203 NP799830.RA7iaoGmMPy0q3rML-Yuhq1SQmc-fFzYq9n__UV6LXPe8130_provenance.