Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP344344.RAAK49ME2M8ll9cLwPJp4FpLSWKk4D0plW25m_n4hDq5A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP344344.RAAK49ME2M8ll9cLwPJp4FpLSWKk4D0plW25m_n4hDq5A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP344344.RAAK49ME2M8ll9cLwPJp4FpLSWKk4D0plW25m_n4hDq5A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP344344.RAAK49ME2M8ll9cLwPJp4FpLSWKk4D0plW25m_n4hDq5A130_provenance.
- NP344344.RAAK49ME2M8ll9cLwPJp4FpLSWKk4D0plW25m_n4hDq5A130_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." NP344344.RAAK49ME2M8ll9cLwPJp4FpLSWKk4D0plW25m_n4hDq5A130_provenance.
- NP344344.RAAK49ME2M8ll9cLwPJp4FpLSWKk4D0plW25m_n4hDq5A130_assertion evidence source_evidence_literature NP344344.RAAK49ME2M8ll9cLwPJp4FpLSWKk4D0plW25m_n4hDq5A130_provenance.
- NP344344.RAAK49ME2M8ll9cLwPJp4FpLSWKk4D0plW25m_n4hDq5A130_assertion SIO_000772 11834590 NP344344.RAAK49ME2M8ll9cLwPJp4FpLSWKk4D0plW25m_n4hDq5A130_provenance.
- NP344344.RAAK49ME2M8ll9cLwPJp4FpLSWKk4D0plW25m_n4hDq5A130_assertion wasDerivedFrom befree-2016 NP344344.RAAK49ME2M8ll9cLwPJp4FpLSWKk4D0plW25m_n4hDq5A130_provenance.
- NP344344.RAAK49ME2M8ll9cLwPJp4FpLSWKk4D0plW25m_n4hDq5A130_assertion wasGeneratedBy ECO_0000203 NP344344.RAAK49ME2M8ll9cLwPJp4FpLSWKk4D0plW25m_n4hDq5A130_provenance.
- befree-2016 importedOn "2016-02-19" NP344344.RAAK49ME2M8ll9cLwPJp4FpLSWKk4D0plW25m_n4hDq5A130_provenance.