Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP910203.RAsBGAC3e98ywqd6VhfnxrQab2zPyTuVhVOQfnOSrQUkI130_assertion> ?p ?o ?g. }
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- NP910203.RAsBGAC3e98ywqd6VhfnxrQab2zPyTuVhVOQfnOSrQUkI130_assertion type Assertion NP910203.RAsBGAC3e98ywqd6VhfnxrQab2zPyTuVhVOQfnOSrQUkI130_head.
- NP910203.RAsBGAC3e98ywqd6VhfnxrQab2zPyTuVhVOQfnOSrQUkI130_assertion wasGeneratedBy ECO_0000203 NP910203.RAsBGAC3e98ywqd6VhfnxrQab2zPyTuVhVOQfnOSrQUkI130_provenance.
- NP910203.RAsBGAC3e98ywqd6VhfnxrQab2zPyTuVhVOQfnOSrQUkI130_assertion wasDerivedFrom befree-20140225 NP910203.RAsBGAC3e98ywqd6VhfnxrQab2zPyTuVhVOQfnOSrQUkI130_provenance.
- NP910203.RAsBGAC3e98ywqd6VhfnxrQab2zPyTuVhVOQfnOSrQUkI130_assertion SIO_000772 23429546 NP910203.RAsBGAC3e98ywqd6VhfnxrQab2zPyTuVhVOQfnOSrQUkI130_provenance.
- NP910203.RAsBGAC3e98ywqd6VhfnxrQab2zPyTuVhVOQfnOSrQUkI130_assertion evidence source_evidence_literature NP910203.RAsBGAC3e98ywqd6VhfnxrQab2zPyTuVhVOQfnOSrQUkI130_provenance.
- NP910203.RAsBGAC3e98ywqd6VhfnxrQab2zPyTuVhVOQfnOSrQUkI130_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." NP910203.RAsBGAC3e98ywqd6VhfnxrQab2zPyTuVhVOQfnOSrQUkI130_provenance.