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- source_evidence_literature type ECO_0000212 NP228501.RA1ElxuVa5MN8wwQRvumFBTQi0zsGGrfy4ZIB-k-nl-6k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP228501.RA1ElxuVa5MN8wwQRvumFBTQi0zsGGrfy4ZIB-k-nl-6k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP228501.RA1ElxuVa5MN8wwQRvumFBTQi0zsGGrfy4ZIB-k-nl-6k130_provenance.
- NP228501.RA1ElxuVa5MN8wwQRvumFBTQi0zsGGrfy4ZIB-k-nl-6k130_assertion description "[Allele frequencies of both the D2S111 and the D2S124 polymorphisms of the SCN2A gene were not significantly different between cases with a specific idiopathic generalized epilepsy subtype (with generalized tonic-clonic seizures) and healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP228501.RA1ElxuVa5MN8wwQRvumFBTQi0zsGGrfy4ZIB-k-nl-6k130_provenance.
- NP228501.RA1ElxuVa5MN8wwQRvumFBTQi0zsGGrfy4ZIB-k-nl-6k130_assertion evidence source_evidence_literature NP228501.RA1ElxuVa5MN8wwQRvumFBTQi0zsGGrfy4ZIB-k-nl-6k130_provenance.
- NP228501.RA1ElxuVa5MN8wwQRvumFBTQi0zsGGrfy4ZIB-k-nl-6k130_assertion SIO_000772 17715289 NP228501.RA1ElxuVa5MN8wwQRvumFBTQi0zsGGrfy4ZIB-k-nl-6k130_provenance.
- NP228501.RA1ElxuVa5MN8wwQRvumFBTQi0zsGGrfy4ZIB-k-nl-6k130_assertion wasDerivedFrom lhgdn-20090331 NP228501.RA1ElxuVa5MN8wwQRvumFBTQi0zsGGrfy4ZIB-k-nl-6k130_provenance.
- NP228501.RA1ElxuVa5MN8wwQRvumFBTQi0zsGGrfy4ZIB-k-nl-6k130_assertion wasGeneratedBy ECO_0000203 NP228501.RA1ElxuVa5MN8wwQRvumFBTQi0zsGGrfy4ZIB-k-nl-6k130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP228501.RA1ElxuVa5MN8wwQRvumFBTQi0zsGGrfy4ZIB-k-nl-6k130_provenance.