Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP371621.RAbZVcWelW5hCiMFO_Vf2-Tzl_PM6ewWv4CNKRNh1IJ5k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP371621.RAbZVcWelW5hCiMFO_Vf2-Tzl_PM6ewWv4CNKRNh1IJ5k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP371621.RAbZVcWelW5hCiMFO_Vf2-Tzl_PM6ewWv4CNKRNh1IJ5k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP371621.RAbZVcWelW5hCiMFO_Vf2-Tzl_PM6ewWv4CNKRNh1IJ5k130_provenance.
- NP371621.RAbZVcWelW5hCiMFO_Vf2-Tzl_PM6ewWv4CNKRNh1IJ5k130_assertion description "[Absence of a functional multidrug resistance protein 2 (MRP2; symbol ABCC2) from the hepatocyte canalicular membrane is the molecular basis of Dubin- Johnson syndrome, an inherited disorder associated with conjugated hyperbilirubinemia in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP371621.RAbZVcWelW5hCiMFO_Vf2-Tzl_PM6ewWv4CNKRNh1IJ5k130_provenance.
- NP371621.RAbZVcWelW5hCiMFO_Vf2-Tzl_PM6ewWv4CNKRNh1IJ5k130_assertion evidence source_evidence_literature NP371621.RAbZVcWelW5hCiMFO_Vf2-Tzl_PM6ewWv4CNKRNh1IJ5k130_provenance.
- NP371621.RAbZVcWelW5hCiMFO_Vf2-Tzl_PM6ewWv4CNKRNh1IJ5k130_assertion SIO_000772 12388192 NP371621.RAbZVcWelW5hCiMFO_Vf2-Tzl_PM6ewWv4CNKRNh1IJ5k130_provenance.
- NP371621.RAbZVcWelW5hCiMFO_Vf2-Tzl_PM6ewWv4CNKRNh1IJ5k130_assertion wasDerivedFrom befree-2016 NP371621.RAbZVcWelW5hCiMFO_Vf2-Tzl_PM6ewWv4CNKRNh1IJ5k130_provenance.
- NP371621.RAbZVcWelW5hCiMFO_Vf2-Tzl_PM6ewWv4CNKRNh1IJ5k130_assertion wasGeneratedBy ECO_0000203 NP371621.RAbZVcWelW5hCiMFO_Vf2-Tzl_PM6ewWv4CNKRNh1IJ5k130_provenance.
- befree-2016 importedOn "2016-02-19" NP371621.RAbZVcWelW5hCiMFO_Vf2-Tzl_PM6ewWv4CNKRNh1IJ5k130_provenance.