Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP853422.RAidUeJwfLrF1Ot7wdpjBfyV9_c2HsVMAWTY8nC0YEORQ130_assertion> ?p ?o ?g. }
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- NP853422.RAidUeJwfLrF1Ot7wdpjBfyV9_c2HsVMAWTY8nC0YEORQ130_assertion type Assertion NP853422.RAidUeJwfLrF1Ot7wdpjBfyV9_c2HsVMAWTY8nC0YEORQ130_head.
- NP853422.RAidUeJwfLrF1Ot7wdpjBfyV9_c2HsVMAWTY8nC0YEORQ130_assertion wasGeneratedBy ECO_0000203 NP853422.RAidUeJwfLrF1Ot7wdpjBfyV9_c2HsVMAWTY8nC0YEORQ130_provenance.
- NP853422.RAidUeJwfLrF1Ot7wdpjBfyV9_c2HsVMAWTY8nC0YEORQ130_assertion wasDerivedFrom befree-20140225 NP853422.RAidUeJwfLrF1Ot7wdpjBfyV9_c2HsVMAWTY8nC0YEORQ130_provenance.
- NP853422.RAidUeJwfLrF1Ot7wdpjBfyV9_c2HsVMAWTY8nC0YEORQ130_assertion SIO_000772 21094958 NP853422.RAidUeJwfLrF1Ot7wdpjBfyV9_c2HsVMAWTY8nC0YEORQ130_provenance.
- NP853422.RAidUeJwfLrF1Ot7wdpjBfyV9_c2HsVMAWTY8nC0YEORQ130_assertion evidence source_evidence_literature NP853422.RAidUeJwfLrF1Ot7wdpjBfyV9_c2HsVMAWTY8nC0YEORQ130_provenance.
- NP853422.RAidUeJwfLrF1Ot7wdpjBfyV9_c2HsVMAWTY8nC0YEORQ130_assertion description "[Gain-of-function mutations in the SCN9A gene (encoding to NaV1.7 voltage-gated sodium channel) cause two rare paroxysmal pain disorders: inherited erythromelalgia (IEM) and paroxysmal extreme pain disorder (PEDP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP853422.RAidUeJwfLrF1Ot7wdpjBfyV9_c2HsVMAWTY8nC0YEORQ130_provenance.