Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP488012.RACeehVPv_cyoAAuzOKHa9bnz_5p58PPFWDIaLZJh-fEM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP488012.RACeehVPv_cyoAAuzOKHa9bnz_5p58PPFWDIaLZJh-fEM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP488012.RACeehVPv_cyoAAuzOKHa9bnz_5p58PPFWDIaLZJh-fEM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP488012.RACeehVPv_cyoAAuzOKHa9bnz_5p58PPFWDIaLZJh-fEM130_provenance.
- NP488012.RACeehVPv_cyoAAuzOKHa9bnz_5p58PPFWDIaLZJh-fEM130_assertion description "[Three individuals (2.6%) with the FRAXA form of the fragile X syndrome and one boy (0.9%) with FRAXE mental retardation were detected; a total of four newly diagnosed fragile X families were identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP488012.RACeehVPv_cyoAAuzOKHa9bnz_5p58PPFWDIaLZJh-fEM130_provenance.
- NP488012.RACeehVPv_cyoAAuzOKHa9bnz_5p58PPFWDIaLZJh-fEM130_assertion evidence source_evidence_literature NP488012.RACeehVPv_cyoAAuzOKHa9bnz_5p58PPFWDIaLZJh-fEM130_provenance.
- NP488012.RACeehVPv_cyoAAuzOKHa9bnz_5p58PPFWDIaLZJh-fEM130_assertion SIO_000772 12113322 NP488012.RACeehVPv_cyoAAuzOKHa9bnz_5p58PPFWDIaLZJh-fEM130_provenance.
- NP488012.RACeehVPv_cyoAAuzOKHa9bnz_5p58PPFWDIaLZJh-fEM130_assertion wasDerivedFrom befree-20140225 NP488012.RACeehVPv_cyoAAuzOKHa9bnz_5p58PPFWDIaLZJh-fEM130_provenance.
- NP488012.RACeehVPv_cyoAAuzOKHa9bnz_5p58PPFWDIaLZJh-fEM130_assertion wasGeneratedBy ECO_0000203 NP488012.RACeehVPv_cyoAAuzOKHa9bnz_5p58PPFWDIaLZJh-fEM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP488012.RACeehVPv_cyoAAuzOKHa9bnz_5p58PPFWDIaLZJh-fEM130_provenance.