Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP437623.RAY7S1m5hoSYtPnPsTOCngeIE5mEcF-r4_EXdd7AsKLlY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP437623.RAY7S1m5hoSYtPnPsTOCngeIE5mEcF-r4_EXdd7AsKLlY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP437623.RAY7S1m5hoSYtPnPsTOCngeIE5mEcF-r4_EXdd7AsKLlY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP437623.RAY7S1m5hoSYtPnPsTOCngeIE5mEcF-r4_EXdd7AsKLlY130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP437623.RAY7S1m5hoSYtPnPsTOCngeIE5mEcF-r4_EXdd7AsKLlY130_provenance.