Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978124.RALLMyZV12FgWnRgNGl1kuVYe579ivTciAaUDjiACFSng130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978124.RALLMyZV12FgWnRgNGl1kuVYe579ivTciAaUDjiACFSng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978124.RALLMyZV12FgWnRgNGl1kuVYe579ivTciAaUDjiACFSng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978124.RALLMyZV12FgWnRgNGl1kuVYe579ivTciAaUDjiACFSng130_provenance.
- NP978124.RALLMyZV12FgWnRgNGl1kuVYe579ivTciAaUDjiACFSng130_assertion description "[ARX is a crucial gene for the development of interneurons in the fetal brain, and a polyalanine expansion mutation of ARX causes mental retardation and seizures, including those of West syndrome, in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978124.RALLMyZV12FgWnRgNGl1kuVYe579ivTciAaUDjiACFSng130_provenance.
- NP978124.RALLMyZV12FgWnRgNGl1kuVYe579ivTciAaUDjiACFSng130_assertion evidence source_evidence_literature NP978124.RALLMyZV12FgWnRgNGl1kuVYe579ivTciAaUDjiACFSng130_provenance.
- NP978124.RALLMyZV12FgWnRgNGl1kuVYe579ivTciAaUDjiACFSng130_assertion SIO_000772 17668384 NP978124.RALLMyZV12FgWnRgNGl1kuVYe579ivTciAaUDjiACFSng130_provenance.
- NP978124.RALLMyZV12FgWnRgNGl1kuVYe579ivTciAaUDjiACFSng130_assertion wasDerivedFrom befree-20150227 NP978124.RALLMyZV12FgWnRgNGl1kuVYe579ivTciAaUDjiACFSng130_provenance.
- NP978124.RALLMyZV12FgWnRgNGl1kuVYe579ivTciAaUDjiACFSng130_assertion wasGeneratedBy ECO_0000203 NP978124.RALLMyZV12FgWnRgNGl1kuVYe579ivTciAaUDjiACFSng130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978124.RALLMyZV12FgWnRgNGl1kuVYe579ivTciAaUDjiACFSng130_provenance.