Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP253474.RA2W98QToHyALPEjPtfEAgv8MQVSRXj0vgV-IIs6XuQls130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP253474.RA2W98QToHyALPEjPtfEAgv8MQVSRXj0vgV-IIs6XuQls130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP253474.RA2W98QToHyALPEjPtfEAgv8MQVSRXj0vgV-IIs6XuQls130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP253474.RA2W98QToHyALPEjPtfEAgv8MQVSRXj0vgV-IIs6XuQls130_provenance.
- befree-2016 importedOn "2016-02-19" NP253474.RA2W98QToHyALPEjPtfEAgv8MQVSRXj0vgV-IIs6XuQls130_provenance.
- 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.