Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP949928.RA4PgiGlkhvO6uInkf7D3eKvZDxs4a0ClWfbmT2s0xpe0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP949928.RA4PgiGlkhvO6uInkf7D3eKvZDxs4a0ClWfbmT2s0xpe0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP949928.RA4PgiGlkhvO6uInkf7D3eKvZDxs4a0ClWfbmT2s0xpe0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP949928.RA4PgiGlkhvO6uInkf7D3eKvZDxs4a0ClWfbmT2s0xpe0130_provenance.
- NP949928.RA4PgiGlkhvO6uInkf7D3eKvZDxs4a0ClWfbmT2s0xpe0130_assertion description "[Functional loss of FMRP causes the inherited intellectual disability fragile X syndrome (FXS), and leads to increased and stimulus-insensitive neuronal protein synthesis in FXS animal models.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP949928.RA4PgiGlkhvO6uInkf7D3eKvZDxs4a0ClWfbmT2s0xpe0130_provenance.
- NP949928.RA4PgiGlkhvO6uInkf7D3eKvZDxs4a0ClWfbmT2s0xpe0130_assertion evidence source_evidence_literature NP949928.RA4PgiGlkhvO6uInkf7D3eKvZDxs4a0ClWfbmT2s0xpe0130_provenance.
- NP949928.RA4PgiGlkhvO6uInkf7D3eKvZDxs4a0ClWfbmT2s0xpe0130_assertion SIO_000772 22207187 NP949928.RA4PgiGlkhvO6uInkf7D3eKvZDxs4a0ClWfbmT2s0xpe0130_provenance.
- NP949928.RA4PgiGlkhvO6uInkf7D3eKvZDxs4a0ClWfbmT2s0xpe0130_assertion wasDerivedFrom befree-2016 NP949928.RA4PgiGlkhvO6uInkf7D3eKvZDxs4a0ClWfbmT2s0xpe0130_provenance.
- NP949928.RA4PgiGlkhvO6uInkf7D3eKvZDxs4a0ClWfbmT2s0xpe0130_assertion wasGeneratedBy ECO_0000203 NP949928.RA4PgiGlkhvO6uInkf7D3eKvZDxs4a0ClWfbmT2s0xpe0130_provenance.
- befree-2016 importedOn "2016-02-19" NP949928.RA4PgiGlkhvO6uInkf7D3eKvZDxs4a0ClWfbmT2s0xpe0130_provenance.