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- source_evidence_literature type ECO_0000212 NP854893.RA6QpXEsMRi7wRFZB-R8SPGd6HikhQepWFzcRjL57T4XM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP854893.RA6QpXEsMRi7wRFZB-R8SPGd6HikhQepWFzcRjL57T4XM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP854893.RA6QpXEsMRi7wRFZB-R8SPGd6HikhQepWFzcRjL57T4XM130_provenance.
- NP854893.RA6QpXEsMRi7wRFZB-R8SPGd6HikhQepWFzcRjL57T4XM130_assertion description "[In this review we discuss the mutation in the fragile X mental retardation-1 gene (FMR1), that leads to FXS, the role FMRP plays in neuronal cells, experiments from our own laboratory that demonstrate reductions of FMRP in additional psychiatric disorders (autism, schizophrenia, bipolar disorder, and major depressive disorder), and potential therapies to ameliorate the loss of FMRP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854893.RA6QpXEsMRi7wRFZB-R8SPGd6HikhQepWFzcRjL57T4XM130_provenance.
- NP854893.RA6QpXEsMRi7wRFZB-R8SPGd6HikhQepWFzcRjL57T4XM130_assertion evidence source_evidence_literature NP854893.RA6QpXEsMRi7wRFZB-R8SPGd6HikhQepWFzcRjL57T4XM130_provenance.
- NP854893.RA6QpXEsMRi7wRFZB-R8SPGd6HikhQepWFzcRjL57T4XM130_assertion SIO_000772 21108954 NP854893.RA6QpXEsMRi7wRFZB-R8SPGd6HikhQepWFzcRjL57T4XM130_provenance.
- NP854893.RA6QpXEsMRi7wRFZB-R8SPGd6HikhQepWFzcRjL57T4XM130_assertion wasDerivedFrom befree-2016 NP854893.RA6QpXEsMRi7wRFZB-R8SPGd6HikhQepWFzcRjL57T4XM130_provenance.
- NP854893.RA6QpXEsMRi7wRFZB-R8SPGd6HikhQepWFzcRjL57T4XM130_assertion wasGeneratedBy ECO_0000203 NP854893.RA6QpXEsMRi7wRFZB-R8SPGd6HikhQepWFzcRjL57T4XM130_provenance.
- befree-2016 importedOn "2016-02-19" NP854893.RA6QpXEsMRi7wRFZB-R8SPGd6HikhQepWFzcRjL57T4XM130_provenance.