Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP508659.RAQtvhkXav-oe1y2S3xGc1fp3_KbrjpdOofSu6o9FMDgA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP508659.RAQtvhkXav-oe1y2S3xGc1fp3_KbrjpdOofSu6o9FMDgA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP508659.RAQtvhkXav-oe1y2S3xGc1fp3_KbrjpdOofSu6o9FMDgA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP508659.RAQtvhkXav-oe1y2S3xGc1fp3_KbrjpdOofSu6o9FMDgA130_provenance.
- NP508659.RAQtvhkXav-oe1y2S3xGc1fp3_KbrjpdOofSu6o9FMDgA130_assertion description "[Fragile X syndrome (FXS) is caused by the transcriptional silencing of the Fmr1 gene, which encodes a protein (FMRP) that can act as a translational suppressor in dendrites, and is characterized by a preponderance of abnormally long, thin and tortuous dendritic spines.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP508659.RAQtvhkXav-oe1y2S3xGc1fp3_KbrjpdOofSu6o9FMDgA130_provenance.
- NP508659.RAQtvhkXav-oe1y2S3xGc1fp3_KbrjpdOofSu6o9FMDgA130_assertion evidence source_evidence_literature NP508659.RAQtvhkXav-oe1y2S3xGc1fp3_KbrjpdOofSu6o9FMDgA130_provenance.
- NP508659.RAQtvhkXav-oe1y2S3xGc1fp3_KbrjpdOofSu6o9FMDgA130_assertion SIO_000772 16098135 NP508659.RAQtvhkXav-oe1y2S3xGc1fp3_KbrjpdOofSu6o9FMDgA130_provenance.
- NP508659.RAQtvhkXav-oe1y2S3xGc1fp3_KbrjpdOofSu6o9FMDgA130_assertion wasDerivedFrom befree-2016 NP508659.RAQtvhkXav-oe1y2S3xGc1fp3_KbrjpdOofSu6o9FMDgA130_provenance.
- NP508659.RAQtvhkXav-oe1y2S3xGc1fp3_KbrjpdOofSu6o9FMDgA130_assertion wasGeneratedBy ECO_0000203 NP508659.RAQtvhkXav-oe1y2S3xGc1fp3_KbrjpdOofSu6o9FMDgA130_provenance.
- befree-2016 importedOn "2016-02-19" NP508659.RAQtvhkXav-oe1y2S3xGc1fp3_KbrjpdOofSu6o9FMDgA130_provenance.