Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP518625.RAgYB8ej2kuEJFKI8Nr7vBtznlCLZg3JU77RNHLVhUJYI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP518625.RAgYB8ej2kuEJFKI8Nr7vBtznlCLZg3JU77RNHLVhUJYI130_assertion type Assertion NP518625.RAgYB8ej2kuEJFKI8Nr7vBtznlCLZg3JU77RNHLVhUJYI130_head.
- NP518625.RAgYB8ej2kuEJFKI8Nr7vBtznlCLZg3JU77RNHLVhUJYI130_assertion description "[Mutations in the human ARX gene have been shown to cause nonsyndromic X-linked mental retardation (MRX) as well as syndromic forms such as X-linked lissencephaly with abnormal genitalia (XLAG), Partington syndrome and X-linked infantile spasm.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP518625.RAgYB8ej2kuEJFKI8Nr7vBtznlCLZg3JU77RNHLVhUJYI130_provenance.
- NP518625.RAgYB8ej2kuEJFKI8Nr7vBtznlCLZg3JU77RNHLVhUJYI130_assertion evidence source_evidence_literature NP518625.RAgYB8ej2kuEJFKI8Nr7vBtznlCLZg3JU77RNHLVhUJYI130_provenance.
- NP518625.RAgYB8ej2kuEJFKI8Nr7vBtznlCLZg3JU77RNHLVhUJYI130_assertion SIO_000772 16235064 NP518625.RAgYB8ej2kuEJFKI8Nr7vBtznlCLZg3JU77RNHLVhUJYI130_provenance.
- NP518625.RAgYB8ej2kuEJFKI8Nr7vBtznlCLZg3JU77RNHLVhUJYI130_assertion wasDerivedFrom befree-2016 NP518625.RAgYB8ej2kuEJFKI8Nr7vBtznlCLZg3JU77RNHLVhUJYI130_provenance.
- NP518625.RAgYB8ej2kuEJFKI8Nr7vBtznlCLZg3JU77RNHLVhUJYI130_assertion wasGeneratedBy ECO_0000203 NP518625.RAgYB8ej2kuEJFKI8Nr7vBtznlCLZg3JU77RNHLVhUJYI130_provenance.