Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP704599.RAfXAQya9ZnG1CkXVIDtri7ERbWXtkGl0AfglBFCXN0VQ130_assertion> ?p ?o ?g. }
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- NP704599.RAfXAQya9ZnG1CkXVIDtri7ERbWXtkGl0AfglBFCXN0VQ130_assertion type Assertion NP704599.RAfXAQya9ZnG1CkXVIDtri7ERbWXtkGl0AfglBFCXN0VQ130_head.
- NP704599.RAfXAQya9ZnG1CkXVIDtri7ERbWXtkGl0AfglBFCXN0VQ130_assertion description "[X-linked lissencephaly with ambiguous genitalia (XLAG) is a recently described genetic disorder caused by mutation in the aristaless-related homeobox (ARX) gene (Xp22.13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP704599.RAfXAQya9ZnG1CkXVIDtri7ERbWXtkGl0AfglBFCXN0VQ130_provenance.
- NP704599.RAfXAQya9ZnG1CkXVIDtri7ERbWXtkGl0AfglBFCXN0VQ130_assertion evidence source_evidence_literature NP704599.RAfXAQya9ZnG1CkXVIDtri7ERbWXtkGl0AfglBFCXN0VQ130_provenance.
- NP704599.RAfXAQya9ZnG1CkXVIDtri7ERbWXtkGl0AfglBFCXN0VQ130_assertion SIO_000772 17221017 NP704599.RAfXAQya9ZnG1CkXVIDtri7ERbWXtkGl0AfglBFCXN0VQ130_provenance.
- NP704599.RAfXAQya9ZnG1CkXVIDtri7ERbWXtkGl0AfglBFCXN0VQ130_assertion wasDerivedFrom befree-20140225 NP704599.RAfXAQya9ZnG1CkXVIDtri7ERbWXtkGl0AfglBFCXN0VQ130_provenance.
- NP704599.RAfXAQya9ZnG1CkXVIDtri7ERbWXtkGl0AfglBFCXN0VQ130_assertion wasGeneratedBy ECO_0000203 NP704599.RAfXAQya9ZnG1CkXVIDtri7ERbWXtkGl0AfglBFCXN0VQ130_provenance.