Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP89677.RAmGDFIvyv9to7psQ2ZJf9VQOqunR4Rq2nPOiYftcEPVo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP89677.RAmGDFIvyv9to7psQ2ZJf9VQOqunR4Rq2nPOiYftcEPVo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP89677.RAmGDFIvyv9to7psQ2ZJf9VQOqunR4Rq2nPOiYftcEPVo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP89677.RAmGDFIvyv9to7psQ2ZJf9VQOqunR4Rq2nPOiYftcEPVo130_provenance.
- NP89677.RAmGDFIvyv9to7psQ2ZJf9VQOqunR4Rq2nPOiYftcEPVo130_assertion description "[Functional impact of global rare copy number variation in autism spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89677.RAmGDFIvyv9to7psQ2ZJf9VQOqunR4Rq2nPOiYftcEPVo130_provenance.
- NP89677.RAmGDFIvyv9to7psQ2ZJf9VQOqunR4Rq2nPOiYftcEPVo130_assertion evidence source_evidence_literature NP89677.RAmGDFIvyv9to7psQ2ZJf9VQOqunR4Rq2nPOiYftcEPVo130_provenance.
- NP89677.RAmGDFIvyv9to7psQ2ZJf9VQOqunR4Rq2nPOiYftcEPVo130_assertion SIO_000772 20531469 NP89677.RAmGDFIvyv9to7psQ2ZJf9VQOqunR4Rq2nPOiYftcEPVo130_provenance.
- NP89677.RAmGDFIvyv9to7psQ2ZJf9VQOqunR4Rq2nPOiYftcEPVo130_assertion wasDerivedFrom gad-20130706 NP89677.RAmGDFIvyv9to7psQ2ZJf9VQOqunR4Rq2nPOiYftcEPVo130_provenance.
- NP89677.RAmGDFIvyv9to7psQ2ZJf9VQOqunR4Rq2nPOiYftcEPVo130_assertion wasGeneratedBy ECO_0000203 NP89677.RAmGDFIvyv9to7psQ2ZJf9VQOqunR4Rq2nPOiYftcEPVo130_provenance.
- gad-20130706 importedOn "2013-07-06" NP89677.RAmGDFIvyv9to7psQ2ZJf9VQOqunR4Rq2nPOiYftcEPVo130_provenance.