Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP782401.RAI4bAsqgE55LA1qZzIThQRtYn5LKh4z00DXQ3JeJGIrY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP782401.RAI4bAsqgE55LA1qZzIThQRtYn5LKh4z00DXQ3JeJGIrY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP782401.RAI4bAsqgE55LA1qZzIThQRtYn5LKh4z00DXQ3JeJGIrY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP782401.RAI4bAsqgE55LA1qZzIThQRtYn5LKh4z00DXQ3JeJGIrY130_provenance.
- NP782401.RAI4bAsqgE55LA1qZzIThQRtYn5LKh4z00DXQ3JeJGIrY130_assertion description "[Association analysis was carried out for 17 single nucleotide polymorphisms (SNPs) covering the genomic GRM4 sequence for all IGE patients as well as for two common IGE subsyndromes [Juvenile Myoclonic Epilepsy (JME, n=215) and Childhood Absence Epilepsy (CAE, n=175)].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782401.RAI4bAsqgE55LA1qZzIThQRtYn5LKh4z00DXQ3JeJGIrY130_provenance.
- NP782401.RAI4bAsqgE55LA1qZzIThQRtYn5LKh4z00DXQ3JeJGIrY130_assertion evidence source_evidence_literature NP782401.RAI4bAsqgE55LA1qZzIThQRtYn5LKh4z00DXQ3JeJGIrY130_provenance.
- NP782401.RAI4bAsqgE55LA1qZzIThQRtYn5LKh4z00DXQ3JeJGIrY130_assertion SIO_000772 20338729 NP782401.RAI4bAsqgE55LA1qZzIThQRtYn5LKh4z00DXQ3JeJGIrY130_provenance.
- NP782401.RAI4bAsqgE55LA1qZzIThQRtYn5LKh4z00DXQ3JeJGIrY130_assertion wasDerivedFrom befree-20140225 NP782401.RAI4bAsqgE55LA1qZzIThQRtYn5LKh4z00DXQ3JeJGIrY130_provenance.
- NP782401.RAI4bAsqgE55LA1qZzIThQRtYn5LKh4z00DXQ3JeJGIrY130_assertion wasGeneratedBy ECO_0000203 NP782401.RAI4bAsqgE55LA1qZzIThQRtYn5LKh4z00DXQ3JeJGIrY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP782401.RAI4bAsqgE55LA1qZzIThQRtYn5LKh4z00DXQ3JeJGIrY130_provenance.