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- source_evidence_literature type ECO_0000212 NP1200166.RA6O-5LqE7vPYNCDf-oIQW4t2bdRuGWtEnPg66c3VFDw4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1200166.RA6O-5LqE7vPYNCDf-oIQW4t2bdRuGWtEnPg66c3VFDw4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1200166.RA6O-5LqE7vPYNCDf-oIQW4t2bdRuGWtEnPg66c3VFDw4130_provenance.
- NP1200166.RA6O-5LqE7vPYNCDf-oIQW4t2bdRuGWtEnPg66c3VFDw4130_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." NP1200166.RA6O-5LqE7vPYNCDf-oIQW4t2bdRuGWtEnPg66c3VFDw4130_provenance.
- NP1200166.RA6O-5LqE7vPYNCDf-oIQW4t2bdRuGWtEnPg66c3VFDw4130_assertion evidence source_evidence_literature NP1200166.RA6O-5LqE7vPYNCDf-oIQW4t2bdRuGWtEnPg66c3VFDw4130_provenance.
- NP1200166.RA6O-5LqE7vPYNCDf-oIQW4t2bdRuGWtEnPg66c3VFDw4130_assertion SIO_000772 25010494 NP1200166.RA6O-5LqE7vPYNCDf-oIQW4t2bdRuGWtEnPg66c3VFDw4130_provenance.
- NP1200166.RA6O-5LqE7vPYNCDf-oIQW4t2bdRuGWtEnPg66c3VFDw4130_assertion wasDerivedFrom befree-2016 NP1200166.RA6O-5LqE7vPYNCDf-oIQW4t2bdRuGWtEnPg66c3VFDw4130_provenance.
- NP1200166.RA6O-5LqE7vPYNCDf-oIQW4t2bdRuGWtEnPg66c3VFDw4130_assertion wasGeneratedBy ECO_0000203 NP1200166.RA6O-5LqE7vPYNCDf-oIQW4t2bdRuGWtEnPg66c3VFDw4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1200166.RA6O-5LqE7vPYNCDf-oIQW4t2bdRuGWtEnPg66c3VFDw4130_provenance.