Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP815105.RAxI0d3rPDVlY5JiESayV2A1feZwpchtmSnlIbClJ_o6Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP815105.RAxI0d3rPDVlY5JiESayV2A1feZwpchtmSnlIbClJ_o6Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP815105.RAxI0d3rPDVlY5JiESayV2A1feZwpchtmSnlIbClJ_o6Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP815105.RAxI0d3rPDVlY5JiESayV2A1feZwpchtmSnlIbClJ_o6Q130_provenance.
- NP815105.RAxI0d3rPDVlY5JiESayV2A1feZwpchtmSnlIbClJ_o6Q130_assertion description "[The Aristaless-related homeobox gene (ARX) is one of the most frequently mutated genes in a spectrum of X-chromosome phenotypes with intellectual disability (ID) as their cardinal feature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP815105.RAxI0d3rPDVlY5JiESayV2A1feZwpchtmSnlIbClJ_o6Q130_provenance.
- NP815105.RAxI0d3rPDVlY5JiESayV2A1feZwpchtmSnlIbClJ_o6Q130_assertion evidence source_evidence_literature NP815105.RAxI0d3rPDVlY5JiESayV2A1feZwpchtmSnlIbClJ_o6Q130_provenance.
- NP815105.RAxI0d3rPDVlY5JiESayV2A1feZwpchtmSnlIbClJ_o6Q130_assertion SIO_000772 20506206 NP815105.RAxI0d3rPDVlY5JiESayV2A1feZwpchtmSnlIbClJ_o6Q130_provenance.
- NP815105.RAxI0d3rPDVlY5JiESayV2A1feZwpchtmSnlIbClJ_o6Q130_assertion wasDerivedFrom befree-2016 NP815105.RAxI0d3rPDVlY5JiESayV2A1feZwpchtmSnlIbClJ_o6Q130_provenance.
- NP815105.RAxI0d3rPDVlY5JiESayV2A1feZwpchtmSnlIbClJ_o6Q130_assertion wasGeneratedBy ECO_0000203 NP815105.RAxI0d3rPDVlY5JiESayV2A1feZwpchtmSnlIbClJ_o6Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP815105.RAxI0d3rPDVlY5JiESayV2A1feZwpchtmSnlIbClJ_o6Q130_provenance.