Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP221978.RAhU_jBF4K_AcgqyW5-qMFEEqyiqORwR8NT1uZ7Z3T2nc130_assertion> ?p ?o ?g. }
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- NP221978.RAhU_jBF4K_AcgqyW5-qMFEEqyiqORwR8NT1uZ7Z3T2nc130_assertion type Assertion NP221978.RAhU_jBF4K_AcgqyW5-qMFEEqyiqORwR8NT1uZ7Z3T2nc130_head.
- NP221978.RAhU_jBF4K_AcgqyW5-qMFEEqyiqORwR8NT1uZ7Z3T2nc130_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." NP221978.RAhU_jBF4K_AcgqyW5-qMFEEqyiqORwR8NT1uZ7Z3T2nc130_provenance.
- NP221978.RAhU_jBF4K_AcgqyW5-qMFEEqyiqORwR8NT1uZ7Z3T2nc130_assertion evidence source_evidence_literature NP221978.RAhU_jBF4K_AcgqyW5-qMFEEqyiqORwR8NT1uZ7Z3T2nc130_provenance.
- NP221978.RAhU_jBF4K_AcgqyW5-qMFEEqyiqORwR8NT1uZ7Z3T2nc130_assertion SIO_000772 17215107 NP221978.RAhU_jBF4K_AcgqyW5-qMFEEqyiqORwR8NT1uZ7Z3T2nc130_provenance.
- NP221978.RAhU_jBF4K_AcgqyW5-qMFEEqyiqORwR8NT1uZ7Z3T2nc130_assertion wasDerivedFrom lhgdn-20090331 NP221978.RAhU_jBF4K_AcgqyW5-qMFEEqyiqORwR8NT1uZ7Z3T2nc130_provenance.
- NP221978.RAhU_jBF4K_AcgqyW5-qMFEEqyiqORwR8NT1uZ7Z3T2nc130_assertion wasGeneratedBy ECO_0000203 NP221978.RAhU_jBF4K_AcgqyW5-qMFEEqyiqORwR8NT1uZ7Z3T2nc130_provenance.