Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP499370.RAYtH86MUNRrgyy95PJnZB1fQamNi6HLdcwoGXGrCXmog130_assertion> ?p ?o ?g. }
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- NP499370.RAYtH86MUNRrgyy95PJnZB1fQamNi6HLdcwoGXGrCXmog130_assertion type Assertion NP499370.RAYtH86MUNRrgyy95PJnZB1fQamNi6HLdcwoGXGrCXmog130_head.
- NP499370.RAYtH86MUNRrgyy95PJnZB1fQamNi6HLdcwoGXGrCXmog130_assertion description "[One family with autosomal dominantly inherited erythermalgia was double heterozygous for two separate SCN9A mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499370.RAYtH86MUNRrgyy95PJnZB1fQamNi6HLdcwoGXGrCXmog130_provenance.
- NP499370.RAYtH86MUNRrgyy95PJnZB1fQamNi6HLdcwoGXGrCXmog130_assertion evidence source_evidence_literature NP499370.RAYtH86MUNRrgyy95PJnZB1fQamNi6HLdcwoGXGrCXmog130_provenance.
- NP499370.RAYtH86MUNRrgyy95PJnZB1fQamNi6HLdcwoGXGrCXmog130_assertion SIO_000772 15955112 NP499370.RAYtH86MUNRrgyy95PJnZB1fQamNi6HLdcwoGXGrCXmog130_provenance.
- NP499370.RAYtH86MUNRrgyy95PJnZB1fQamNi6HLdcwoGXGrCXmog130_assertion wasDerivedFrom befree-2016 NP499370.RAYtH86MUNRrgyy95PJnZB1fQamNi6HLdcwoGXGrCXmog130_provenance.
- NP499370.RAYtH86MUNRrgyy95PJnZB1fQamNi6HLdcwoGXGrCXmog130_assertion wasGeneratedBy ECO_0000203 NP499370.RAYtH86MUNRrgyy95PJnZB1fQamNi6HLdcwoGXGrCXmog130_provenance.