Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978086.RAwoEHplraVwmBNaEbR0DT8IgmLlQgZC4e0IMrcn0NnOY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978086.RAwoEHplraVwmBNaEbR0DT8IgmLlQgZC4e0IMrcn0NnOY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978086.RAwoEHplraVwmBNaEbR0DT8IgmLlQgZC4e0IMrcn0NnOY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978086.RAwoEHplraVwmBNaEbR0DT8IgmLlQgZC4e0IMrcn0NnOY130_provenance.
- NP978086.RAwoEHplraVwmBNaEbR0DT8IgmLlQgZC4e0IMrcn0NnOY130_assertion description "[Aristaless-related homeobox (ARX) gene mutations cause a diverse spectrum of disorders of the human brain, including lissencephaly, various forms of epilepsy and non-syndromic mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978086.RAwoEHplraVwmBNaEbR0DT8IgmLlQgZC4e0IMrcn0NnOY130_provenance.
- NP978086.RAwoEHplraVwmBNaEbR0DT8IgmLlQgZC4e0IMrcn0NnOY130_assertion evidence source_evidence_literature NP978086.RAwoEHplraVwmBNaEbR0DT8IgmLlQgZC4e0IMrcn0NnOY130_provenance.
- NP978086.RAwoEHplraVwmBNaEbR0DT8IgmLlQgZC4e0IMrcn0NnOY130_assertion SIO_000772 19738637 NP978086.RAwoEHplraVwmBNaEbR0DT8IgmLlQgZC4e0IMrcn0NnOY130_provenance.
- NP978086.RAwoEHplraVwmBNaEbR0DT8IgmLlQgZC4e0IMrcn0NnOY130_assertion wasDerivedFrom befree-20150227 NP978086.RAwoEHplraVwmBNaEbR0DT8IgmLlQgZC4e0IMrcn0NnOY130_provenance.
- NP978086.RAwoEHplraVwmBNaEbR0DT8IgmLlQgZC4e0IMrcn0NnOY130_assertion wasGeneratedBy ECO_0000203 NP978086.RAwoEHplraVwmBNaEbR0DT8IgmLlQgZC4e0IMrcn0NnOY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978086.RAwoEHplraVwmBNaEbR0DT8IgmLlQgZC4e0IMrcn0NnOY130_provenance.