Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP253474.RA2W98QToHyALPEjPtfEAgv8MQVSRXj0vgV-IIs6XuQls130_assertion> ?p ?o ?g. }
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- NP253474.RA2W98QToHyALPEjPtfEAgv8MQVSRXj0vgV-IIs6XuQls130_assertion type Assertion NP253474.RA2W98QToHyALPEjPtfEAgv8MQVSRXj0vgV-IIs6XuQls130_head.
- NP253474.RA2W98QToHyALPEjPtfEAgv8MQVSRXj0vgV-IIs6XuQls130_assertion wasGeneratedBy ECO_0000203 NP253474.RA2W98QToHyALPEjPtfEAgv8MQVSRXj0vgV-IIs6XuQls130_provenance.
- NP253474.RA2W98QToHyALPEjPtfEAgv8MQVSRXj0vgV-IIs6XuQls130_assertion wasDerivedFrom befree-2016 NP253474.RA2W98QToHyALPEjPtfEAgv8MQVSRXj0vgV-IIs6XuQls130_provenance.
- NP253474.RA2W98QToHyALPEjPtfEAgv8MQVSRXj0vgV-IIs6XuQls130_assertion SIO_000772 10341296 NP253474.RA2W98QToHyALPEjPtfEAgv8MQVSRXj0vgV-IIs6XuQls130_provenance.
- NP253474.RA2W98QToHyALPEjPtfEAgv8MQVSRXj0vgV-IIs6XuQls130_assertion evidence source_evidence_literature NP253474.RA2W98QToHyALPEjPtfEAgv8MQVSRXj0vgV-IIs6XuQls130_provenance.
- NP253474.RA2W98QToHyALPEjPtfEAgv8MQVSRXj0vgV-IIs6XuQls130_assertion description "[Fragile X syndrome is the most common form of inherited mental retardation currently known, associated with a wide range of developmental disabilities in both males and females, caused by a large expansion of a (CGG)n repeat in the first exon of the FMR1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253474.RA2W98QToHyALPEjPtfEAgv8MQVSRXj0vgV-IIs6XuQls130_provenance.