Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP499370.RAYtH86MUNRrgyy95PJnZB1fQamNi6HLdcwoGXGrCXmog130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP499370.RAYtH86MUNRrgyy95PJnZB1fQamNi6HLdcwoGXGrCXmog130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP499370.RAYtH86MUNRrgyy95PJnZB1fQamNi6HLdcwoGXGrCXmog130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP499370.RAYtH86MUNRrgyy95PJnZB1fQamNi6HLdcwoGXGrCXmog130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP499370.RAYtH86MUNRrgyy95PJnZB1fQamNi6HLdcwoGXGrCXmog130_provenance.