Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP640243.RAo55r7D5e4PfOzEC6t7T3X940PfKkbdoG5hQBROgOjJk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP640243.RAo55r7D5e4PfOzEC6t7T3X940PfKkbdoG5hQBROgOjJk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP640243.RAo55r7D5e4PfOzEC6t7T3X940PfKkbdoG5hQBROgOjJk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP640243.RAo55r7D5e4PfOzEC6t7T3X940PfKkbdoG5hQBROgOjJk130_provenance.
- NP640243.RAo55r7D5e4PfOzEC6t7T3X940PfKkbdoG5hQBROgOjJk130_assertion description "[We examined expression of MDR1 and MRP1 in refractory epilepsy from three common causes, dysembryoplastic neuroepithelial tumours (DNTs; eight cases), focal cortical dysplasia (FCD; 14 cases) and hippocampal sclerosis (HS; eight cases).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP640243.RAo55r7D5e4PfOzEC6t7T3X940PfKkbdoG5hQBROgOjJk130_provenance.
- NP640243.RAo55r7D5e4PfOzEC6t7T3X940PfKkbdoG5hQBROgOjJk130_assertion evidence source_evidence_literature NP640243.RAo55r7D5e4PfOzEC6t7T3X940PfKkbdoG5hQBROgOjJk130_provenance.
- NP640243.RAo55r7D5e4PfOzEC6t7T3X940PfKkbdoG5hQBROgOjJk130_assertion SIO_000772 11834590 NP640243.RAo55r7D5e4PfOzEC6t7T3X940PfKkbdoG5hQBROgOjJk130_provenance.
- NP640243.RAo55r7D5e4PfOzEC6t7T3X940PfKkbdoG5hQBROgOjJk130_assertion wasDerivedFrom befree-20140225 NP640243.RAo55r7D5e4PfOzEC6t7T3X940PfKkbdoG5hQBROgOjJk130_provenance.
- NP640243.RAo55r7D5e4PfOzEC6t7T3X940PfKkbdoG5hQBROgOjJk130_assertion wasGeneratedBy ECO_0000203 NP640243.RAo55r7D5e4PfOzEC6t7T3X940PfKkbdoG5hQBROgOjJk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP640243.RAo55r7D5e4PfOzEC6t7T3X940PfKkbdoG5hQBROgOjJk130_provenance.