Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP501080.RAZ4eYyKaEKVEbvhOX0H10kA8gKxaVy5l893FDEvjpnYA130_assertion> ?p ?o ?g. }
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- NP501080.RAZ4eYyKaEKVEbvhOX0H10kA8gKxaVy5l893FDEvjpnYA130_assertion type Assertion NP501080.RAZ4eYyKaEKVEbvhOX0H10kA8gKxaVy5l893FDEvjpnYA130_head.
- NP501080.RAZ4eYyKaEKVEbvhOX0H10kA8gKxaVy5l893FDEvjpnYA130_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." NP501080.RAZ4eYyKaEKVEbvhOX0H10kA8gKxaVy5l893FDEvjpnYA130_provenance.
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- NP501080.RAZ4eYyKaEKVEbvhOX0H10kA8gKxaVy5l893FDEvjpnYA130_assertion SIO_000772 21108954 NP501080.RAZ4eYyKaEKVEbvhOX0H10kA8gKxaVy5l893FDEvjpnYA130_provenance.
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