Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_assertion type Assertion NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_head.
- NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_assertion description "[ARX gene mutations have been known as important causes of developmental and neurological disorders and are responsible for a large spectrum of abnormal phenotypes, includeing syndromic as well as nonsyndromic forms of mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_provenance.
- NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_assertion evidence source_evidence_literature NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_provenance.
- NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_assertion SIO_000772 16845484 NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_provenance.
- NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_assertion wasDerivedFrom befree-2016 NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_provenance.
- NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_assertion wasGeneratedBy ECO_0000203 NP560002.RARKXAOQk52Af3JwH0PsjDp72jGJ8fJKwMSShtbmvxRIo130_provenance.