Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP752800.RApdTuB6pN4oreaWJt0Js_SXcz-D325AJYcqZDJwzn6EY130_assertion> ?p ?o ?g. }
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- NP752800.RApdTuB6pN4oreaWJt0Js_SXcz-D325AJYcqZDJwzn6EY130_assertion type Assertion NP752800.RApdTuB6pN4oreaWJt0Js_SXcz-D325AJYcqZDJwzn6EY130_head.
- NP752800.RApdTuB6pN4oreaWJt0Js_SXcz-D325AJYcqZDJwzn6EY130_assertion description "[Our results confirm that congenital Rett syndrome can be caused by copy-number variation in FOXG1 and expand the clinical phenotypic spectrum of FOXG1 defect in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP752800.RApdTuB6pN4oreaWJt0Js_SXcz-D325AJYcqZDJwzn6EY130_provenance.
- NP752800.RApdTuB6pN4oreaWJt0Js_SXcz-D325AJYcqZDJwzn6EY130_assertion evidence source_evidence_literature NP752800.RApdTuB6pN4oreaWJt0Js_SXcz-D325AJYcqZDJwzn6EY130_provenance.
- NP752800.RApdTuB6pN4oreaWJt0Js_SXcz-D325AJYcqZDJwzn6EY130_assertion SIO_000772 19623215 NP752800.RApdTuB6pN4oreaWJt0Js_SXcz-D325AJYcqZDJwzn6EY130_provenance.
- NP752800.RApdTuB6pN4oreaWJt0Js_SXcz-D325AJYcqZDJwzn6EY130_assertion wasDerivedFrom befree-2016 NP752800.RApdTuB6pN4oreaWJt0Js_SXcz-D325AJYcqZDJwzn6EY130_provenance.
- NP752800.RApdTuB6pN4oreaWJt0Js_SXcz-D325AJYcqZDJwzn6EY130_assertion wasGeneratedBy ECO_0000203 NP752800.RApdTuB6pN4oreaWJt0Js_SXcz-D325AJYcqZDJwzn6EY130_provenance.