Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP142250.RAl6rNnl_mY-7RsRU1v61j6StneLWzuRDUPTPpUq3OAOU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP142250.RAl6rNnl_mY-7RsRU1v61j6StneLWzuRDUPTPpUq3OAOU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP142250.RAl6rNnl_mY-7RsRU1v61j6StneLWzuRDUPTPpUq3OAOU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP142250.RAl6rNnl_mY-7RsRU1v61j6StneLWzuRDUPTPpUq3OAOU130_provenance.
- NP142250.RAl6rNnl_mY-7RsRU1v61j6StneLWzuRDUPTPpUq3OAOU130_assertion description "[study failed to replicate an association of the common GABRB3 exon 1a promoter SNP rs4906902 with childhood absence epilepsy.no evidence that the common functional C-variant confers a substantial epileptogenic effect to a broad spectrum of IGE syndromes ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP142250.RAl6rNnl_mY-7RsRU1v61j6StneLWzuRDUPTPpUq3OAOU130_provenance.
- NP142250.RAl6rNnl_mY-7RsRU1v61j6StneLWzuRDUPTPpUq3OAOU130_assertion evidence source_evidence_literature NP142250.RAl6rNnl_mY-7RsRU1v61j6StneLWzuRDUPTPpUq3OAOU130_provenance.
- NP142250.RAl6rNnl_mY-7RsRU1v61j6StneLWzuRDUPTPpUq3OAOU130_assertion SIO_000772 17215107 NP142250.RAl6rNnl_mY-7RsRU1v61j6StneLWzuRDUPTPpUq3OAOU130_provenance.
- NP142250.RAl6rNnl_mY-7RsRU1v61j6StneLWzuRDUPTPpUq3OAOU130_assertion wasDerivedFrom lhgdn-20090331 NP142250.RAl6rNnl_mY-7RsRU1v61j6StneLWzuRDUPTPpUq3OAOU130_provenance.
- NP142250.RAl6rNnl_mY-7RsRU1v61j6StneLWzuRDUPTPpUq3OAOU130_assertion wasGeneratedBy ECO_0000203 NP142250.RAl6rNnl_mY-7RsRU1v61j6StneLWzuRDUPTPpUq3OAOU130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP142250.RAl6rNnl_mY-7RsRU1v61j6StneLWzuRDUPTPpUq3OAOU130_provenance.