Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP439207.RAvPWo9nQIG76_RGwZM-Bq_lOX7O9cGFZ2b9r2_xMG2ng130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP439207.RAvPWo9nQIG76_RGwZM-Bq_lOX7O9cGFZ2b9r2_xMG2ng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP439207.RAvPWo9nQIG76_RGwZM-Bq_lOX7O9cGFZ2b9r2_xMG2ng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP439207.RAvPWo9nQIG76_RGwZM-Bq_lOX7O9cGFZ2b9r2_xMG2ng130_provenance.
- NP439207.RAvPWo9nQIG76_RGwZM-Bq_lOX7O9cGFZ2b9r2_xMG2ng130_assertion wasGeneratedBy ECO_0000203 NP439207.RAvPWo9nQIG76_RGwZM-Bq_lOX7O9cGFZ2b9r2_xMG2ng130_provenance.
- NP439207.RAvPWo9nQIG76_RGwZM-Bq_lOX7O9cGFZ2b9r2_xMG2ng130_assertion wasDerivedFrom befree-20140225 NP439207.RAvPWo9nQIG76_RGwZM-Bq_lOX7O9cGFZ2b9r2_xMG2ng130_provenance.
- NP439207.RAvPWo9nQIG76_RGwZM-Bq_lOX7O9cGFZ2b9r2_xMG2ng130_assertion SIO_000772 17855451 NP439207.RAvPWo9nQIG76_RGwZM-Bq_lOX7O9cGFZ2b9r2_xMG2ng130_provenance.
- NP439207.RAvPWo9nQIG76_RGwZM-Bq_lOX7O9cGFZ2b9r2_xMG2ng130_assertion evidence source_evidence_literature NP439207.RAvPWo9nQIG76_RGwZM-Bq_lOX7O9cGFZ2b9r2_xMG2ng130_provenance.
- NP439207.RAvPWo9nQIG76_RGwZM-Bq_lOX7O9cGFZ2b9r2_xMG2ng130_assertion description "[Failure to properly terminate SOX10 translation causes the generation of a deleterious functional domain that occurs because of translation of the normal 3'-UTR; the mutant fusion protein causes a severe neurological disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP439207.RAvPWo9nQIG76_RGwZM-Bq_lOX7O9cGFZ2b9r2_xMG2ng130_provenance.
- befree-20140225 importedOn "2014-02-25" NP439207.RAvPWo9nQIG76_RGwZM-Bq_lOX7O9cGFZ2b9r2_xMG2ng130_provenance.