Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP409068.RAbb__egcWhFzG4hVkJiiDVT2uRIffDwqtxw19FyWsO-E130_assertion> ?p ?o ?g. }
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- NP409068.RAbb__egcWhFzG4hVkJiiDVT2uRIffDwqtxw19FyWsO-E130_assertion type Assertion NP409068.RAbb__egcWhFzG4hVkJiiDVT2uRIffDwqtxw19FyWsO-E130_head.
- NP409068.RAbb__egcWhFzG4hVkJiiDVT2uRIffDwqtxw19FyWsO-E130_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." NP409068.RAbb__egcWhFzG4hVkJiiDVT2uRIffDwqtxw19FyWsO-E130_provenance.
- NP409068.RAbb__egcWhFzG4hVkJiiDVT2uRIffDwqtxw19FyWsO-E130_assertion evidence source_evidence_literature NP409068.RAbb__egcWhFzG4hVkJiiDVT2uRIffDwqtxw19FyWsO-E130_provenance.
- NP409068.RAbb__egcWhFzG4hVkJiiDVT2uRIffDwqtxw19FyWsO-E130_assertion SIO_000772 21108954 NP409068.RAbb__egcWhFzG4hVkJiiDVT2uRIffDwqtxw19FyWsO-E130_provenance.
- NP409068.RAbb__egcWhFzG4hVkJiiDVT2uRIffDwqtxw19FyWsO-E130_assertion wasDerivedFrom befree-20150227 NP409068.RAbb__egcWhFzG4hVkJiiDVT2uRIffDwqtxw19FyWsO-E130_provenance.
- NP409068.RAbb__egcWhFzG4hVkJiiDVT2uRIffDwqtxw19FyWsO-E130_assertion wasGeneratedBy ECO_0000203 NP409068.RAbb__egcWhFzG4hVkJiiDVT2uRIffDwqtxw19FyWsO-E130_provenance.