Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP500569.RAl4ChLtyFQTQKYcObdyV24dUpHBPbrGd9AGL8A2XhdYs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP500569.RAl4ChLtyFQTQKYcObdyV24dUpHBPbrGd9AGL8A2XhdYs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP500569.RAl4ChLtyFQTQKYcObdyV24dUpHBPbrGd9AGL8A2XhdYs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP500569.RAl4ChLtyFQTQKYcObdyV24dUpHBPbrGd9AGL8A2XhdYs130_provenance.
- NP500569.RAl4ChLtyFQTQKYcObdyV24dUpHBPbrGd9AGL8A2XhdYs130_assertion description "[FRAXE (FMR2) is a fragile site associated with mental impairment located in Xq28, 600 kb distal to FRAXA (FMR1), the fragile X syndrome fragile site.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500569.RAl4ChLtyFQTQKYcObdyV24dUpHBPbrGd9AGL8A2XhdYs130_provenance.
- NP500569.RAl4ChLtyFQTQKYcObdyV24dUpHBPbrGd9AGL8A2XhdYs130_assertion evidence source_evidence_literature NP500569.RAl4ChLtyFQTQKYcObdyV24dUpHBPbrGd9AGL8A2XhdYs130_provenance.
- NP500569.RAl4ChLtyFQTQKYcObdyV24dUpHBPbrGd9AGL8A2XhdYs130_assertion SIO_000772 11462240 NP500569.RAl4ChLtyFQTQKYcObdyV24dUpHBPbrGd9AGL8A2XhdYs130_provenance.
- NP500569.RAl4ChLtyFQTQKYcObdyV24dUpHBPbrGd9AGL8A2XhdYs130_assertion wasDerivedFrom befree-20140225 NP500569.RAl4ChLtyFQTQKYcObdyV24dUpHBPbrGd9AGL8A2XhdYs130_provenance.
- NP500569.RAl4ChLtyFQTQKYcObdyV24dUpHBPbrGd9AGL8A2XhdYs130_assertion wasGeneratedBy ECO_0000203 NP500569.RAl4ChLtyFQTQKYcObdyV24dUpHBPbrGd9AGL8A2XhdYs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP500569.RAl4ChLtyFQTQKYcObdyV24dUpHBPbrGd9AGL8A2XhdYs130_provenance.