Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP437623.RAY7S1m5hoSYtPnPsTOCngeIE5mEcF-r4_EXdd7AsKLlY130_assertion> ?p ?o ?g. }
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- NP437623.RAY7S1m5hoSYtPnPsTOCngeIE5mEcF-r4_EXdd7AsKLlY130_assertion type Assertion NP437623.RAY7S1m5hoSYtPnPsTOCngeIE5mEcF-r4_EXdd7AsKLlY130_head.
- NP437623.RAY7S1m5hoSYtPnPsTOCngeIE5mEcF-r4_EXdd7AsKLlY130_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." NP437623.RAY7S1m5hoSYtPnPsTOCngeIE5mEcF-r4_EXdd7AsKLlY130_provenance.
- NP437623.RAY7S1m5hoSYtPnPsTOCngeIE5mEcF-r4_EXdd7AsKLlY130_assertion evidence source_evidence_literature NP437623.RAY7S1m5hoSYtPnPsTOCngeIE5mEcF-r4_EXdd7AsKLlY130_provenance.
- NP437623.RAY7S1m5hoSYtPnPsTOCngeIE5mEcF-r4_EXdd7AsKLlY130_assertion SIO_000772 19623215 NP437623.RAY7S1m5hoSYtPnPsTOCngeIE5mEcF-r4_EXdd7AsKLlY130_provenance.
- NP437623.RAY7S1m5hoSYtPnPsTOCngeIE5mEcF-r4_EXdd7AsKLlY130_assertion wasDerivedFrom befree-20140225 NP437623.RAY7S1m5hoSYtPnPsTOCngeIE5mEcF-r4_EXdd7AsKLlY130_provenance.
- NP437623.RAY7S1m5hoSYtPnPsTOCngeIE5mEcF-r4_EXdd7AsKLlY130_assertion wasGeneratedBy ECO_0000203 NP437623.RAY7S1m5hoSYtPnPsTOCngeIE5mEcF-r4_EXdd7AsKLlY130_provenance.