Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP344346.RAhjcLLssmP0DHVJOk0vfuxFZcNdyYta1sehI_VwVtcd4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP344346.RAhjcLLssmP0DHVJOk0vfuxFZcNdyYta1sehI_VwVtcd4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP344346.RAhjcLLssmP0DHVJOk0vfuxFZcNdyYta1sehI_VwVtcd4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP344346.RAhjcLLssmP0DHVJOk0vfuxFZcNdyYta1sehI_VwVtcd4130_provenance.
- NP344346.RAhjcLLssmP0DHVJOk0vfuxFZcNdyYta1sehI_VwVtcd4130_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." NP344346.RAhjcLLssmP0DHVJOk0vfuxFZcNdyYta1sehI_VwVtcd4130_provenance.
- NP344346.RAhjcLLssmP0DHVJOk0vfuxFZcNdyYta1sehI_VwVtcd4130_assertion evidence source_evidence_literature NP344346.RAhjcLLssmP0DHVJOk0vfuxFZcNdyYta1sehI_VwVtcd4130_provenance.
- NP344346.RAhjcLLssmP0DHVJOk0vfuxFZcNdyYta1sehI_VwVtcd4130_assertion SIO_000772 11834590 NP344346.RAhjcLLssmP0DHVJOk0vfuxFZcNdyYta1sehI_VwVtcd4130_provenance.
- NP344346.RAhjcLLssmP0DHVJOk0vfuxFZcNdyYta1sehI_VwVtcd4130_assertion wasDerivedFrom befree-2016 NP344346.RAhjcLLssmP0DHVJOk0vfuxFZcNdyYta1sehI_VwVtcd4130_provenance.
- NP344346.RAhjcLLssmP0DHVJOk0vfuxFZcNdyYta1sehI_VwVtcd4130_assertion wasGeneratedBy ECO_0000203 NP344346.RAhjcLLssmP0DHVJOk0vfuxFZcNdyYta1sehI_VwVtcd4130_provenance.
- befree-2016 importedOn "2016-02-19" NP344346.RAhjcLLssmP0DHVJOk0vfuxFZcNdyYta1sehI_VwVtcd4130_provenance.