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- source_evidence_literature type ECO_0000212 NP947667.RAvTHrRka3ze5rHg8okJaCST5fJuPVfsW-4Ey1DXS7Oh4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP947667.RAvTHrRka3ze5rHg8okJaCST5fJuPVfsW-4Ey1DXS7Oh4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP947667.RAvTHrRka3ze5rHg8okJaCST5fJuPVfsW-4Ey1DXS7Oh4130_provenance.
- NP947667.RAvTHrRka3ze5rHg8okJaCST5fJuPVfsW-4Ey1DXS7Oh4130_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." NP947667.RAvTHrRka3ze5rHg8okJaCST5fJuPVfsW-4Ey1DXS7Oh4130_provenance.
- NP947667.RAvTHrRka3ze5rHg8okJaCST5fJuPVfsW-4Ey1DXS7Oh4130_assertion evidence source_evidence_literature NP947667.RAvTHrRka3ze5rHg8okJaCST5fJuPVfsW-4Ey1DXS7Oh4130_provenance.
- NP947667.RAvTHrRka3ze5rHg8okJaCST5fJuPVfsW-4Ey1DXS7Oh4130_assertion SIO_000772 25010494 NP947667.RAvTHrRka3ze5rHg8okJaCST5fJuPVfsW-4Ey1DXS7Oh4130_provenance.
- NP947667.RAvTHrRka3ze5rHg8okJaCST5fJuPVfsW-4Ey1DXS7Oh4130_assertion wasDerivedFrom befree-20150227 NP947667.RAvTHrRka3ze5rHg8okJaCST5fJuPVfsW-4Ey1DXS7Oh4130_provenance.
- NP947667.RAvTHrRka3ze5rHg8okJaCST5fJuPVfsW-4Ey1DXS7Oh4130_assertion wasGeneratedBy ECO_0000203 NP947667.RAvTHrRka3ze5rHg8okJaCST5fJuPVfsW-4Ey1DXS7Oh4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP947667.RAvTHrRka3ze5rHg8okJaCST5fJuPVfsW-4Ey1DXS7Oh4130_provenance.