Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1200168.RAwNwN90K2BYLp_jfPniOlRHUY5zvICtKKxJkgXTUa9fY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1200168.RAwNwN90K2BYLp_jfPniOlRHUY5zvICtKKxJkgXTUa9fY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1200168.RAwNwN90K2BYLp_jfPniOlRHUY5zvICtKKxJkgXTUa9fY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1200168.RAwNwN90K2BYLp_jfPniOlRHUY5zvICtKKxJkgXTUa9fY130_provenance.
- NP1200168.RAwNwN90K2BYLp_jfPniOlRHUY5zvICtKKxJkgXTUa9fY130_assertion description "[By creating new Pcnxl2 frameshift alleles using TALEN mutagenesis, we show that Pcnxl2 deficiency is responsible for mitigating the seizure phenotype - making Pcnxl2 the first known modifier gene for absence seizures in any species.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1200168.RAwNwN90K2BYLp_jfPniOlRHUY5zvICtKKxJkgXTUa9fY130_provenance.
- NP1200168.RAwNwN90K2BYLp_jfPniOlRHUY5zvICtKKxJkgXTUa9fY130_assertion evidence source_evidence_literature NP1200168.RAwNwN90K2BYLp_jfPniOlRHUY5zvICtKKxJkgXTUa9fY130_provenance.
- NP1200168.RAwNwN90K2BYLp_jfPniOlRHUY5zvICtKKxJkgXTUa9fY130_assertion SIO_000772 25010494 NP1200168.RAwNwN90K2BYLp_jfPniOlRHUY5zvICtKKxJkgXTUa9fY130_provenance.
- NP1200168.RAwNwN90K2BYLp_jfPniOlRHUY5zvICtKKxJkgXTUa9fY130_assertion wasDerivedFrom befree-2016 NP1200168.RAwNwN90K2BYLp_jfPniOlRHUY5zvICtKKxJkgXTUa9fY130_provenance.
- NP1200168.RAwNwN90K2BYLp_jfPniOlRHUY5zvICtKKxJkgXTUa9fY130_assertion wasGeneratedBy ECO_0000203 NP1200168.RAwNwN90K2BYLp_jfPniOlRHUY5zvICtKKxJkgXTUa9fY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1200168.RAwNwN90K2BYLp_jfPniOlRHUY5zvICtKKxJkgXTUa9fY130_provenance.