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- source_evidence_literature type ECO_0000212 NP978221.RAZDVfFVy7dzFcRwnCB6g71HNbj-P0FOg5AYj7v9CRXK4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978221.RAZDVfFVy7dzFcRwnCB6g71HNbj-P0FOg5AYj7v9CRXK4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978221.RAZDVfFVy7dzFcRwnCB6g71HNbj-P0FOg5AYj7v9CRXK4130_provenance.
- NP978221.RAZDVfFVy7dzFcRwnCB6g71HNbj-P0FOg5AYj7v9CRXK4130_assertion description "[Mutations in the ARX gene, at Xp22.3, cause several disorders, including infantile spasms, X-linked lissencephaly with abnormal genitalia (XLAG), callosal agenesis and isolated intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978221.RAZDVfFVy7dzFcRwnCB6g71HNbj-P0FOg5AYj7v9CRXK4130_provenance.
- NP978221.RAZDVfFVy7dzFcRwnCB6g71HNbj-P0FOg5AYj7v9CRXK4130_assertion evidence source_evidence_literature NP978221.RAZDVfFVy7dzFcRwnCB6g71HNbj-P0FOg5AYj7v9CRXK4130_provenance.
- NP978221.RAZDVfFVy7dzFcRwnCB6g71HNbj-P0FOg5AYj7v9CRXK4130_assertion SIO_000772 22585566 NP978221.RAZDVfFVy7dzFcRwnCB6g71HNbj-P0FOg5AYj7v9CRXK4130_provenance.
- NP978221.RAZDVfFVy7dzFcRwnCB6g71HNbj-P0FOg5AYj7v9CRXK4130_assertion wasDerivedFrom befree-20150227 NP978221.RAZDVfFVy7dzFcRwnCB6g71HNbj-P0FOg5AYj7v9CRXK4130_provenance.
- NP978221.RAZDVfFVy7dzFcRwnCB6g71HNbj-P0FOg5AYj7v9CRXK4130_assertion wasGeneratedBy ECO_0000203 NP978221.RAZDVfFVy7dzFcRwnCB6g71HNbj-P0FOg5AYj7v9CRXK4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978221.RAZDVfFVy7dzFcRwnCB6g71HNbj-P0FOg5AYj7v9CRXK4130_provenance.