Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP629616.RAp97hBHtK3de_nXmsTYJUbk3y7FI394NSGPQ4Hxnvlqo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP629616.RAp97hBHtK3de_nXmsTYJUbk3y7FI394NSGPQ4Hxnvlqo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP629616.RAp97hBHtK3de_nXmsTYJUbk3y7FI394NSGPQ4Hxnvlqo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP629616.RAp97hBHtK3de_nXmsTYJUbk3y7FI394NSGPQ4Hxnvlqo130_provenance.
- NP629616.RAp97hBHtK3de_nXmsTYJUbk3y7FI394NSGPQ4Hxnvlqo130_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." NP629616.RAp97hBHtK3de_nXmsTYJUbk3y7FI394NSGPQ4Hxnvlqo130_provenance.
- NP629616.RAp97hBHtK3de_nXmsTYJUbk3y7FI394NSGPQ4Hxnvlqo130_assertion evidence source_evidence_literature NP629616.RAp97hBHtK3de_nXmsTYJUbk3y7FI394NSGPQ4Hxnvlqo130_provenance.
- NP629616.RAp97hBHtK3de_nXmsTYJUbk3y7FI394NSGPQ4Hxnvlqo130_assertion SIO_000772 21108954 NP629616.RAp97hBHtK3de_nXmsTYJUbk3y7FI394NSGPQ4Hxnvlqo130_provenance.
- NP629616.RAp97hBHtK3de_nXmsTYJUbk3y7FI394NSGPQ4Hxnvlqo130_assertion wasDerivedFrom befree-20140225 NP629616.RAp97hBHtK3de_nXmsTYJUbk3y7FI394NSGPQ4Hxnvlqo130_provenance.
- NP629616.RAp97hBHtK3de_nXmsTYJUbk3y7FI394NSGPQ4Hxnvlqo130_assertion wasGeneratedBy ECO_0000203 NP629616.RAp97hBHtK3de_nXmsTYJUbk3y7FI394NSGPQ4Hxnvlqo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP629616.RAp97hBHtK3de_nXmsTYJUbk3y7FI394NSGPQ4Hxnvlqo130_provenance.