Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP338874.RAJdbtnNH1DR5VY-Nsr0ZNREdGjdJq-350pyLaZ-TdHYg130_assertion> ?p ?o ?g. }
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- NP338874.RAJdbtnNH1DR5VY-Nsr0ZNREdGjdJq-350pyLaZ-TdHYg130_assertion type Assertion NP338874.RAJdbtnNH1DR5VY-Nsr0ZNREdGjdJq-350pyLaZ-TdHYg130_head.
- NP338874.RAJdbtnNH1DR5VY-Nsr0ZNREdGjdJq-350pyLaZ-TdHYg130_assertion description "[Association analysis was carried out for 17 single nucleotide polymorphisms (SNPs) covering the genomic GRM4 sequence for all IGE patients as well as for two common IGE subsyndromes [Juvenile Myoclonic Epilepsy (JME, n=215) and Childhood Absence Epilepsy (CAE, n=175)].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP338874.RAJdbtnNH1DR5VY-Nsr0ZNREdGjdJq-350pyLaZ-TdHYg130_provenance.
- NP338874.RAJdbtnNH1DR5VY-Nsr0ZNREdGjdJq-350pyLaZ-TdHYg130_assertion evidence source_evidence_literature NP338874.RAJdbtnNH1DR5VY-Nsr0ZNREdGjdJq-350pyLaZ-TdHYg130_provenance.
- NP338874.RAJdbtnNH1DR5VY-Nsr0ZNREdGjdJq-350pyLaZ-TdHYg130_assertion SIO_000772 20338729 NP338874.RAJdbtnNH1DR5VY-Nsr0ZNREdGjdJq-350pyLaZ-TdHYg130_provenance.
- NP338874.RAJdbtnNH1DR5VY-Nsr0ZNREdGjdJq-350pyLaZ-TdHYg130_assertion wasDerivedFrom befree-20140225 NP338874.RAJdbtnNH1DR5VY-Nsr0ZNREdGjdJq-350pyLaZ-TdHYg130_provenance.
- NP338874.RAJdbtnNH1DR5VY-Nsr0ZNREdGjdJq-350pyLaZ-TdHYg130_assertion wasGeneratedBy ECO_0000203 NP338874.RAJdbtnNH1DR5VY-Nsr0ZNREdGjdJq-350pyLaZ-TdHYg130_provenance.