Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP618884.RA0V2RjpNxR4OoXt-288y2EMsQ0ubXGoYm5eGt1uDqqp8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP618884.RA0V2RjpNxR4OoXt-288y2EMsQ0ubXGoYm5eGt1uDqqp8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP618884.RA0V2RjpNxR4OoXt-288y2EMsQ0ubXGoYm5eGt1uDqqp8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP618884.RA0V2RjpNxR4OoXt-288y2EMsQ0ubXGoYm5eGt1uDqqp8130_provenance.
- NP618884.RA0V2RjpNxR4OoXt-288y2EMsQ0ubXGoYm5eGt1uDqqp8130_assertion description "[Mutations in the Aristaless-related homeobox (ARX) gene are associated with pleiotropic phenotypes including infantile spasms, mental retardation and dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP618884.RA0V2RjpNxR4OoXt-288y2EMsQ0ubXGoYm5eGt1uDqqp8130_provenance.
- NP618884.RA0V2RjpNxR4OoXt-288y2EMsQ0ubXGoYm5eGt1uDqqp8130_assertion evidence source_evidence_literature NP618884.RA0V2RjpNxR4OoXt-288y2EMsQ0ubXGoYm5eGt1uDqqp8130_provenance.
- NP618884.RA0V2RjpNxR4OoXt-288y2EMsQ0ubXGoYm5eGt1uDqqp8130_assertion SIO_000772 18823727 NP618884.RA0V2RjpNxR4OoXt-288y2EMsQ0ubXGoYm5eGt1uDqqp8130_provenance.
- NP618884.RA0V2RjpNxR4OoXt-288y2EMsQ0ubXGoYm5eGt1uDqqp8130_assertion wasDerivedFrom befree-20140225 NP618884.RA0V2RjpNxR4OoXt-288y2EMsQ0ubXGoYm5eGt1uDqqp8130_provenance.
- NP618884.RA0V2RjpNxR4OoXt-288y2EMsQ0ubXGoYm5eGt1uDqqp8130_assertion wasGeneratedBy ECO_0000203 NP618884.RA0V2RjpNxR4OoXt-288y2EMsQ0ubXGoYm5eGt1uDqqp8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP618884.RA0V2RjpNxR4OoXt-288y2EMsQ0ubXGoYm5eGt1uDqqp8130_provenance.