Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
Showing items 1 to 3 of
3
with 100 items per page.
- 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." provenance.
- NP137864.RAXYuR2ee-0gB4RukUB51lzlm0SQktv2ql2BUwI-p5nh4130_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." NP137864.RAXYuR2ee-0gB4RukUB51lzlm0SQktv2ql2BUwI-p5nh4130_provenance.
- NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0130_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." NP168309.RAdKsLIyhT0presPDrb17atc3D28A5ANEgFaxzWeXogR0130_provenance.