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- source_evidence_literature type ECO_0000212 NP640915.RApELzDNl13yRcBR19Ak5L_gNP38cxCEXVpx68QrGX7gY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP640915.RApELzDNl13yRcBR19Ak5L_gNP38cxCEXVpx68QrGX7gY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP640915.RApELzDNl13yRcBR19Ak5L_gNP38cxCEXVpx68QrGX7gY130_provenance.
- befree-2016 importedOn "2016-02-19" NP640915.RApELzDNl13yRcBR19Ak5L_gNP38cxCEXVpx68QrGX7gY130_provenance.
- NP640915.RApELzDNl13yRcBR19Ak5L_gNP38cxCEXVpx68QrGX7gY130_assertion wasGeneratedBy ECO_0000203 NP640915.RApELzDNl13yRcBR19Ak5L_gNP38cxCEXVpx68QrGX7gY130_provenance.
- NP640915.RApELzDNl13yRcBR19Ak5L_gNP38cxCEXVpx68QrGX7gY130_assertion wasDerivedFrom befree-2016 NP640915.RApELzDNl13yRcBR19Ak5L_gNP38cxCEXVpx68QrGX7gY130_provenance.
- NP640915.RApELzDNl13yRcBR19Ak5L_gNP38cxCEXVpx68QrGX7gY130_assertion SIO_000772 18021921 NP640915.RApELzDNl13yRcBR19Ak5L_gNP38cxCEXVpx68QrGX7gY130_provenance.
- NP640915.RApELzDNl13yRcBR19Ak5L_gNP38cxCEXVpx68QrGX7gY130_assertion evidence source_evidence_literature NP640915.RApELzDNl13yRcBR19Ak5L_gNP38cxCEXVpx68QrGX7gY130_provenance.
- NP640915.RApELzDNl13yRcBR19Ak5L_gNP38cxCEXVpx68QrGX7gY130_assertion description "[Although SCN1A, the gene encoding the neuronal voltage-gated sodium channel, type 1A, is a well-recognized target of mutations underlying a spectrum of epilepsy syndromes, and lies within an extended 12-Mb disease-associated haplotype at the familial hemiplegic migraine-3 locus, it remains to be confirmed that mutations within this gene itself cause syndromes that include migraine phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP640915.RApELzDNl13yRcBR19Ak5L_gNP38cxCEXVpx68QrGX7gY130_provenance.