Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP137864.RAXYuR2ee-0gB4RukUB51lzlm0SQktv2ql2BUwI-p5nh4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP137864.RAXYuR2ee-0gB4RukUB51lzlm0SQktv2ql2BUwI-p5nh4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP137864.RAXYuR2ee-0gB4RukUB51lzlm0SQktv2ql2BUwI-p5nh4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP137864.RAXYuR2ee-0gB4RukUB51lzlm0SQktv2ql2BUwI-p5nh4130_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.
- NP137864.RAXYuR2ee-0gB4RukUB51lzlm0SQktv2ql2BUwI-p5nh4130_assertion evidence source_evidence_literature NP137864.RAXYuR2ee-0gB4RukUB51lzlm0SQktv2ql2BUwI-p5nh4130_provenance.
- NP137864.RAXYuR2ee-0gB4RukUB51lzlm0SQktv2ql2BUwI-p5nh4130_assertion SIO_000772 20338729 NP137864.RAXYuR2ee-0gB4RukUB51lzlm0SQktv2ql2BUwI-p5nh4130_provenance.
- NP137864.RAXYuR2ee-0gB4RukUB51lzlm0SQktv2ql2BUwI-p5nh4130_assertion wasDerivedFrom gad-20150221 NP137864.RAXYuR2ee-0gB4RukUB51lzlm0SQktv2ql2BUwI-p5nh4130_provenance.
- NP137864.RAXYuR2ee-0gB4RukUB51lzlm0SQktv2ql2BUwI-p5nh4130_assertion wasGeneratedBy ECO_0000203 NP137864.RAXYuR2ee-0gB4RukUB51lzlm0SQktv2ql2BUwI-p5nh4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP137864.RAXYuR2ee-0gB4RukUB51lzlm0SQktv2ql2BUwI-p5nh4130_provenance.