Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP65061.RA6W4uGtjojGTsj2GQOGaLsz-n7WBNSwjZ-FjCfTRoWI8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP65061.RA6W4uGtjojGTsj2GQOGaLsz-n7WBNSwjZ-FjCfTRoWI8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP65061.RA6W4uGtjojGTsj2GQOGaLsz-n7WBNSwjZ-FjCfTRoWI8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP65061.RA6W4uGtjojGTsj2GQOGaLsz-n7WBNSwjZ-FjCfTRoWI8130_provenance.
- gad-20150221 importedOn "2015-02-21" NP65061.RA6W4uGtjojGTsj2GQOGaLsz-n7WBNSwjZ-FjCfTRoWI8130_provenance.
- NP65061.RA6W4uGtjojGTsj2GQOGaLsz-n7WBNSwjZ-FjCfTRoWI8130_assertion wasGeneratedBy ECO_0000203 NP65061.RA6W4uGtjojGTsj2GQOGaLsz-n7WBNSwjZ-FjCfTRoWI8130_provenance.
- NP65061.RA6W4uGtjojGTsj2GQOGaLsz-n7WBNSwjZ-FjCfTRoWI8130_assertion wasDerivedFrom gad-20150221 NP65061.RA6W4uGtjojGTsj2GQOGaLsz-n7WBNSwjZ-FjCfTRoWI8130_provenance.
- NP65061.RA6W4uGtjojGTsj2GQOGaLsz-n7WBNSwjZ-FjCfTRoWI8130_assertion SIO_000772 11254445 NP65061.RA6W4uGtjojGTsj2GQOGaLsz-n7WBNSwjZ-FjCfTRoWI8130_provenance.
- NP65061.RA6W4uGtjojGTsj2GQOGaLsz-n7WBNSwjZ-FjCfTRoWI8130_assertion evidence source_evidence_literature NP65061.RA6W4uGtjojGTsj2GQOGaLsz-n7WBNSwjZ-FjCfTRoWI8130_provenance.
- NP65061.RA6W4uGtjojGTsj2GQOGaLsz-n7WBNSwjZ-FjCfTRoWI8130_assertion description "[Although a few candidate disease alleles were identified, the patient survey suggests that SCN1A is not a major contributor to idiopathic generalized epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65061.RA6W4uGtjojGTsj2GQOGaLsz-n7WBNSwjZ-FjCfTRoWI8130_provenance.