Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP924763.RACbmBW38hLXMkp7PpEwKsyrRpRUUdX0dP5Te7DBkA5mI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP924763.RACbmBW38hLXMkp7PpEwKsyrRpRUUdX0dP5Te7DBkA5mI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP924763.RACbmBW38hLXMkp7PpEwKsyrRpRUUdX0dP5Te7DBkA5mI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP924763.RACbmBW38hLXMkp7PpEwKsyrRpRUUdX0dP5Te7DBkA5mI130_provenance.
- befree-2016 importedOn "2016-02-19" NP924763.RACbmBW38hLXMkp7PpEwKsyrRpRUUdX0dP5Te7DBkA5mI130_provenance.
- NP924763.RACbmBW38hLXMkp7PpEwKsyrRpRUUdX0dP5Te7DBkA5mI130_assertion wasGeneratedBy ECO_0000203 NP924763.RACbmBW38hLXMkp7PpEwKsyrRpRUUdX0dP5Te7DBkA5mI130_provenance.
- NP924763.RACbmBW38hLXMkp7PpEwKsyrRpRUUdX0dP5Te7DBkA5mI130_assertion wasDerivedFrom befree-2016 NP924763.RACbmBW38hLXMkp7PpEwKsyrRpRUUdX0dP5Te7DBkA5mI130_provenance.
- NP924763.RACbmBW38hLXMkp7PpEwKsyrRpRUUdX0dP5Te7DBkA5mI130_assertion SIO_000772 21930553 NP924763.RACbmBW38hLXMkp7PpEwKsyrRpRUUdX0dP5Te7DBkA5mI130_provenance.
- NP924763.RACbmBW38hLXMkp7PpEwKsyrRpRUUdX0dP5Te7DBkA5mI130_assertion evidence source_evidence_literature NP924763.RACbmBW38hLXMkp7PpEwKsyrRpRUUdX0dP5Te7DBkA5mI130_provenance.
- NP924763.RACbmBW38hLXMkp7PpEwKsyrRpRUUdX0dP5Te7DBkA5mI130_assertion description "[A child with mild X-linked intellectual disability and a microduplication at Xp22.12 including RPS6KA3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924763.RACbmBW38hLXMkp7PpEwKsyrRpRUUdX0dP5Te7DBkA5mI130_provenance.