Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP155784.RADMInnJmWpKBnAw-8gflM9vPqCH1fch7JZlCyDYBLhJ8130_assertion> ?p ?o ?g. }
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- NP155784.RADMInnJmWpKBnAw-8gflM9vPqCH1fch7JZlCyDYBLhJ8130_assertion type Assertion NP155784.RADMInnJmWpKBnAw-8gflM9vPqCH1fch7JZlCyDYBLhJ8130_head.
- NP155784.RADMInnJmWpKBnAw-8gflM9vPqCH1fch7JZlCyDYBLhJ8130_assertion description "[Mutations in the Aristaless-related homeobox gene (ARX) are associated with a wide variety of neurologic disorders including lissencephaly, hydrocephaly, West syndrome, Partington syndrome, and X-linked intellectual disability with or without epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP155784.RADMInnJmWpKBnAw-8gflM9vPqCH1fch7JZlCyDYBLhJ8130_provenance.
- NP155784.RADMInnJmWpKBnAw-8gflM9vPqCH1fch7JZlCyDYBLhJ8130_assertion evidence source_evidence_literature NP155784.RADMInnJmWpKBnAw-8gflM9vPqCH1fch7JZlCyDYBLhJ8130_provenance.
- NP155784.RADMInnJmWpKBnAw-8gflM9vPqCH1fch7JZlCyDYBLhJ8130_assertion SIO_000772 22252899 NP155784.RADMInnJmWpKBnAw-8gflM9vPqCH1fch7JZlCyDYBLhJ8130_provenance.
- NP155784.RADMInnJmWpKBnAw-8gflM9vPqCH1fch7JZlCyDYBLhJ8130_assertion wasDerivedFrom befree-20140225 NP155784.RADMInnJmWpKBnAw-8gflM9vPqCH1fch7JZlCyDYBLhJ8130_provenance.
- NP155784.RADMInnJmWpKBnAw-8gflM9vPqCH1fch7JZlCyDYBLhJ8130_assertion wasGeneratedBy ECO_0000203 NP155784.RADMInnJmWpKBnAw-8gflM9vPqCH1fch7JZlCyDYBLhJ8130_provenance.