Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP796126.RAXjEVVcV5_cE1GVhSpdtTzEqcqR2-HWiafTahML-Licc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP796126.RAXjEVVcV5_cE1GVhSpdtTzEqcqR2-HWiafTahML-Licc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP796126.RAXjEVVcV5_cE1GVhSpdtTzEqcqR2-HWiafTahML-Licc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP796126.RAXjEVVcV5_cE1GVhSpdtTzEqcqR2-HWiafTahML-Licc130_provenance.
- NP796126.RAXjEVVcV5_cE1GVhSpdtTzEqcqR2-HWiafTahML-Licc130_assertion description "[Linkage studies of families ascertained through patients with juvenile myoclonic epilepsy (JME) suggest that an HLA-linked susceptibility gene on chromosome 6, designated `EJM1,` predisposes to a group of idiopathic generalized epilepsies (IGEs) comprising JME, juvenile absence epilepsy (JAE), childhood absence epilepsies (CAE), and epilepsies with generalized tonic-clonic seizures (GTCS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP796126.RAXjEVVcV5_cE1GVhSpdtTzEqcqR2-HWiafTahML-Licc130_provenance.
- NP796126.RAXjEVVcV5_cE1GVhSpdtTzEqcqR2-HWiafTahML-Licc130_assertion evidence source_evidence_literature NP796126.RAXjEVVcV5_cE1GVhSpdtTzEqcqR2-HWiafTahML-Licc130_provenance.
- NP796126.RAXjEVVcV5_cE1GVhSpdtTzEqcqR2-HWiafTahML-Licc130_assertion SIO_000772 7654068 NP796126.RAXjEVVcV5_cE1GVhSpdtTzEqcqR2-HWiafTahML-Licc130_provenance.
- NP796126.RAXjEVVcV5_cE1GVhSpdtTzEqcqR2-HWiafTahML-Licc130_assertion wasDerivedFrom befree-20140225 NP796126.RAXjEVVcV5_cE1GVhSpdtTzEqcqR2-HWiafTahML-Licc130_provenance.
- NP796126.RAXjEVVcV5_cE1GVhSpdtTzEqcqR2-HWiafTahML-Licc130_assertion wasGeneratedBy ECO_0000203 NP796126.RAXjEVVcV5_cE1GVhSpdtTzEqcqR2-HWiafTahML-Licc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP796126.RAXjEVVcV5_cE1GVhSpdtTzEqcqR2-HWiafTahML-Licc130_provenance.