Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_provenance.
- NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_assertion description "[Aristaless-related homeobox gene (ARX) mutation leads to several neurological disorders including X-linked lissencephaly with abnormal genitalia (XLAG), West syndrome and Partington syndrome, with XLAG being the most severe form.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_provenance.
- NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_assertion evidence source_evidence_literature NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_provenance.
- NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_assertion SIO_000772 20538404 NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_provenance.
- NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_assertion wasDerivedFrom befree-20140225 NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_provenance.
- NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_assertion wasGeneratedBy ECO_0000203 NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_provenance.