Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP49826.RAxDjujrqM-GJZcxADsrxnmFhOmNNs8sluotiQXNVeXV4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP49826.RAxDjujrqM-GJZcxADsrxnmFhOmNNs8sluotiQXNVeXV4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP49826.RAxDjujrqM-GJZcxADsrxnmFhOmNNs8sluotiQXNVeXV4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP49826.RAxDjujrqM-GJZcxADsrxnmFhOmNNs8sluotiQXNVeXV4130_provenance.
- NP49826.RAxDjujrqM-GJZcxADsrxnmFhOmNNs8sluotiQXNVeXV4130_assertion description "[We cannot exclude an association of ABCB1 variants on P-gp function, but our results suggest that brain ABCB1 mRNA and protein expression is not substantially influenced by major ABCB1 genetic variants thus explaining in part results from case-control studies obtaining lack of association of ABCB1 polymorphisms to the risk of refractory epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49826.RAxDjujrqM-GJZcxADsrxnmFhOmNNs8sluotiQXNVeXV4130_provenance.
- NP49826.RAxDjujrqM-GJZcxADsrxnmFhOmNNs8sluotiQXNVeXV4130_assertion evidence source_evidence_literature NP49826.RAxDjujrqM-GJZcxADsrxnmFhOmNNs8sluotiQXNVeXV4130_provenance.
- NP49826.RAxDjujrqM-GJZcxADsrxnmFhOmNNs8sluotiQXNVeXV4130_assertion SIO_000772 18494787 NP49826.RAxDjujrqM-GJZcxADsrxnmFhOmNNs8sluotiQXNVeXV4130_provenance.
- NP49826.RAxDjujrqM-GJZcxADsrxnmFhOmNNs8sluotiQXNVeXV4130_assertion wasDerivedFrom gad-20130706 NP49826.RAxDjujrqM-GJZcxADsrxnmFhOmNNs8sluotiQXNVeXV4130_provenance.
- NP49826.RAxDjujrqM-GJZcxADsrxnmFhOmNNs8sluotiQXNVeXV4130_assertion wasGeneratedBy ECO_0000203 NP49826.RAxDjujrqM-GJZcxADsrxnmFhOmNNs8sluotiQXNVeXV4130_provenance.
- gad-20130706 importedOn "2013-07-06" NP49826.RAxDjujrqM-GJZcxADsrxnmFhOmNNs8sluotiQXNVeXV4130_provenance.