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- source_evidence_literature type ECO_0000212 NP978114.RA9dx4stPeh94eWIaC2aflLHj4FAFVGWylsFiNlms16bY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978114.RA9dx4stPeh94eWIaC2aflLHj4FAFVGWylsFiNlms16bY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978114.RA9dx4stPeh94eWIaC2aflLHj4FAFVGWylsFiNlms16bY130_provenance.
- NP978114.RA9dx4stPeh94eWIaC2aflLHj4FAFVGWylsFiNlms16bY130_assertion description "[Mutations in the Aristaless-related homeobox gene (ARX) are associated with a wide variety of neurologic disorders including lissencephaly, hydrocephaly, West syndrome, Partington syndrome, and X-linked intellectual disability with or without epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978114.RA9dx4stPeh94eWIaC2aflLHj4FAFVGWylsFiNlms16bY130_provenance.
- NP978114.RA9dx4stPeh94eWIaC2aflLHj4FAFVGWylsFiNlms16bY130_assertion evidence source_evidence_literature NP978114.RA9dx4stPeh94eWIaC2aflLHj4FAFVGWylsFiNlms16bY130_provenance.
- NP978114.RA9dx4stPeh94eWIaC2aflLHj4FAFVGWylsFiNlms16bY130_assertion SIO_000772 22252899 NP978114.RA9dx4stPeh94eWIaC2aflLHj4FAFVGWylsFiNlms16bY130_provenance.
- NP978114.RA9dx4stPeh94eWIaC2aflLHj4FAFVGWylsFiNlms16bY130_assertion wasDerivedFrom befree-20150227 NP978114.RA9dx4stPeh94eWIaC2aflLHj4FAFVGWylsFiNlms16bY130_provenance.
- NP978114.RA9dx4stPeh94eWIaC2aflLHj4FAFVGWylsFiNlms16bY130_assertion wasGeneratedBy ECO_0000203 NP978114.RA9dx4stPeh94eWIaC2aflLHj4FAFVGWylsFiNlms16bY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978114.RA9dx4stPeh94eWIaC2aflLHj4FAFVGWylsFiNlms16bY130_provenance.