Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP314195.RA0A1VMSYgClCQb3D1QObebrTTkaXx0pEotg-hIQS9gGo130_assertion> ?p ?o ?g. }
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- NP314195.RA0A1VMSYgClCQb3D1QObebrTTkaXx0pEotg-hIQS9gGo130_assertion type Assertion NP314195.RA0A1VMSYgClCQb3D1QObebrTTkaXx0pEotg-hIQS9gGo130_head.
- NP314195.RA0A1VMSYgClCQb3D1QObebrTTkaXx0pEotg-hIQS9gGo130_assertion description "[Array comparative genomic hybridization (CGH) demonstrated a 1.5-Mb terminal deletion of the long arm of chromosome 20, which included deletion of the KCNQ2 and CHRNA4 genes, both of which have been associated with specific epilepsy syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314195.RA0A1VMSYgClCQb3D1QObebrTTkaXx0pEotg-hIQS9gGo130_provenance.
- NP314195.RA0A1VMSYgClCQb3D1QObebrTTkaXx0pEotg-hIQS9gGo130_assertion evidence source_evidence_literature NP314195.RA0A1VMSYgClCQb3D1QObebrTTkaXx0pEotg-hIQS9gGo130_provenance.
- NP314195.RA0A1VMSYgClCQb3D1QObebrTTkaXx0pEotg-hIQS9gGo130_assertion SIO_000772 23166088 NP314195.RA0A1VMSYgClCQb3D1QObebrTTkaXx0pEotg-hIQS9gGo130_provenance.
- NP314195.RA0A1VMSYgClCQb3D1QObebrTTkaXx0pEotg-hIQS9gGo130_assertion wasDerivedFrom befree-20150227 NP314195.RA0A1VMSYgClCQb3D1QObebrTTkaXx0pEotg-hIQS9gGo130_provenance.
- NP314195.RA0A1VMSYgClCQb3D1QObebrTTkaXx0pEotg-hIQS9gGo130_assertion wasGeneratedBy ECO_0000203 NP314195.RA0A1VMSYgClCQb3D1QObebrTTkaXx0pEotg-hIQS9gGo130_provenance.