Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP408692.RAAXK5e6nILEjDHuTEgUhBJ9WGmZRdwaq0_Eh9OdD5DjE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP408692.RAAXK5e6nILEjDHuTEgUhBJ9WGmZRdwaq0_Eh9OdD5DjE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP408692.RAAXK5e6nILEjDHuTEgUhBJ9WGmZRdwaq0_Eh9OdD5DjE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP408692.RAAXK5e6nILEjDHuTEgUhBJ9WGmZRdwaq0_Eh9OdD5DjE130_provenance.
- NP408692.RAAXK5e6nILEjDHuTEgUhBJ9WGmZRdwaq0_Eh9OdD5DjE130_assertion description "[Thus, FXS can be considered a disorder of synaptic plasticity, and a developmental disorder in the purest sense: mutation of the FMR1 (fragile X mental retardation 1) gene results in abnormal synaptic development in response to experience.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408692.RAAXK5e6nILEjDHuTEgUhBJ9WGmZRdwaq0_Eh9OdD5DjE130_provenance.
- NP408692.RAAXK5e6nILEjDHuTEgUhBJ9WGmZRdwaq0_Eh9OdD5DjE130_assertion evidence source_evidence_literature NP408692.RAAXK5e6nILEjDHuTEgUhBJ9WGmZRdwaq0_Eh9OdD5DjE130_provenance.
- NP408692.RAAXK5e6nILEjDHuTEgUhBJ9WGmZRdwaq0_Eh9OdD5DjE130_assertion SIO_000772 21893938 NP408692.RAAXK5e6nILEjDHuTEgUhBJ9WGmZRdwaq0_Eh9OdD5DjE130_provenance.
- NP408692.RAAXK5e6nILEjDHuTEgUhBJ9WGmZRdwaq0_Eh9OdD5DjE130_assertion wasDerivedFrom befree-20150227 NP408692.RAAXK5e6nILEjDHuTEgUhBJ9WGmZRdwaq0_Eh9OdD5DjE130_provenance.
- NP408692.RAAXK5e6nILEjDHuTEgUhBJ9WGmZRdwaq0_Eh9OdD5DjE130_assertion wasGeneratedBy ECO_0000203 NP408692.RAAXK5e6nILEjDHuTEgUhBJ9WGmZRdwaq0_Eh9OdD5DjE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP408692.RAAXK5e6nILEjDHuTEgUhBJ9WGmZRdwaq0_Eh9OdD5DjE130_provenance.