Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1054801.RAIPgdaTO8pv-xACTLopPBnf-_5FqVbg4F0sCrhbQVOFw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1054801.RAIPgdaTO8pv-xACTLopPBnf-_5FqVbg4F0sCrhbQVOFw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1054801.RAIPgdaTO8pv-xACTLopPBnf-_5FqVbg4F0sCrhbQVOFw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1054801.RAIPgdaTO8pv-xACTLopPBnf-_5FqVbg4F0sCrhbQVOFw130_provenance.
- NP1054801.RAIPgdaTO8pv-xACTLopPBnf-_5FqVbg4F0sCrhbQVOFw130_assertion description "[A genome-wide association study in idiopathic generalized epilepsy revealed the first common risk variants for human seizure disorders including variants in VRK2, PNPO and SCN1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1054801.RAIPgdaTO8pv-xACTLopPBnf-_5FqVbg4F0sCrhbQVOFw130_provenance.
- NP1054801.RAIPgdaTO8pv-xACTLopPBnf-_5FqVbg4F0sCrhbQVOFw130_assertion evidence source_evidence_literature NP1054801.RAIPgdaTO8pv-xACTLopPBnf-_5FqVbg4F0sCrhbQVOFw130_provenance.
- NP1054801.RAIPgdaTO8pv-xACTLopPBnf-_5FqVbg4F0sCrhbQVOFw130_assertion SIO_000772 23429546 NP1054801.RAIPgdaTO8pv-xACTLopPBnf-_5FqVbg4F0sCrhbQVOFw130_provenance.
- NP1054801.RAIPgdaTO8pv-xACTLopPBnf-_5FqVbg4F0sCrhbQVOFw130_assertion wasDerivedFrom befree-2016 NP1054801.RAIPgdaTO8pv-xACTLopPBnf-_5FqVbg4F0sCrhbQVOFw130_provenance.
- NP1054801.RAIPgdaTO8pv-xACTLopPBnf-_5FqVbg4F0sCrhbQVOFw130_assertion wasGeneratedBy ECO_0000203 NP1054801.RAIPgdaTO8pv-xACTLopPBnf-_5FqVbg4F0sCrhbQVOFw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1054801.RAIPgdaTO8pv-xACTLopPBnf-_5FqVbg4F0sCrhbQVOFw130_provenance.