Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP256895.RAhm6FYWcZ0oEJ01JnlGUEbYBUWYsdPWRNL1DUs5dSTWg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP256895.RAhm6FYWcZ0oEJ01JnlGUEbYBUWYsdPWRNL1DUs5dSTWg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP256895.RAhm6FYWcZ0oEJ01JnlGUEbYBUWYsdPWRNL1DUs5dSTWg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP256895.RAhm6FYWcZ0oEJ01JnlGUEbYBUWYsdPWRNL1DUs5dSTWg130_provenance.
- NP256895.RAhm6FYWcZ0oEJ01JnlGUEbYBUWYsdPWRNL1DUs5dSTWg130_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." NP256895.RAhm6FYWcZ0oEJ01JnlGUEbYBUWYsdPWRNL1DUs5dSTWg130_provenance.
- NP256895.RAhm6FYWcZ0oEJ01JnlGUEbYBUWYsdPWRNL1DUs5dSTWg130_assertion evidence source_evidence_literature NP256895.RAhm6FYWcZ0oEJ01JnlGUEbYBUWYsdPWRNL1DUs5dSTWg130_provenance.
- NP256895.RAhm6FYWcZ0oEJ01JnlGUEbYBUWYsdPWRNL1DUs5dSTWg130_assertion SIO_000772 17668384 NP256895.RAhm6FYWcZ0oEJ01JnlGUEbYBUWYsdPWRNL1DUs5dSTWg130_provenance.
- NP256895.RAhm6FYWcZ0oEJ01JnlGUEbYBUWYsdPWRNL1DUs5dSTWg130_assertion wasDerivedFrom befree-20140225 NP256895.RAhm6FYWcZ0oEJ01JnlGUEbYBUWYsdPWRNL1DUs5dSTWg130_provenance.
- NP256895.RAhm6FYWcZ0oEJ01JnlGUEbYBUWYsdPWRNL1DUs5dSTWg130_assertion wasGeneratedBy ECO_0000203 NP256895.RAhm6FYWcZ0oEJ01JnlGUEbYBUWYsdPWRNL1DUs5dSTWg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP256895.RAhm6FYWcZ0oEJ01JnlGUEbYBUWYsdPWRNL1DUs5dSTWg130_provenance.