Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP718067.RAbp2e3O3IpEXpECNniQEVmG_TqvrK836dtaB1yPT9F6Q130_assertion> ?p ?o ?g. }
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- NP718067.RAbp2e3O3IpEXpECNniQEVmG_TqvrK836dtaB1yPT9F6Q130_assertion type Assertion NP718067.RAbp2e3O3IpEXpECNniQEVmG_TqvrK836dtaB1yPT9F6Q130_head.
- NP718067.RAbp2e3O3IpEXpECNniQEVmG_TqvrK836dtaB1yPT9F6Q130_assertion description "[Dubin-Johnson syndrome (DJS) is an inherited disorder characterized by conjugated hyperbilirubinemia and is caused by mutations of the canalicular multispecific organic anion transporter (cMOAT)/ multidrug resistance protein 2 (MRP2)/ ATP-binding cassette, sub-family C, member 2 (ABCC2) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718067.RAbp2e3O3IpEXpECNniQEVmG_TqvrK836dtaB1yPT9F6Q130_provenance.
- NP718067.RAbp2e3O3IpEXpECNniQEVmG_TqvrK836dtaB1yPT9F6Q130_assertion evidence source_evidence_literature NP718067.RAbp2e3O3IpEXpECNniQEVmG_TqvrK836dtaB1yPT9F6Q130_provenance.
- NP718067.RAbp2e3O3IpEXpECNniQEVmG_TqvrK836dtaB1yPT9F6Q130_assertion SIO_000772 12087194 NP718067.RAbp2e3O3IpEXpECNniQEVmG_TqvrK836dtaB1yPT9F6Q130_provenance.
- NP718067.RAbp2e3O3IpEXpECNniQEVmG_TqvrK836dtaB1yPT9F6Q130_assertion wasDerivedFrom befree-20140225 NP718067.RAbp2e3O3IpEXpECNniQEVmG_TqvrK836dtaB1yPT9F6Q130_provenance.
- NP718067.RAbp2e3O3IpEXpECNniQEVmG_TqvrK836dtaB1yPT9F6Q130_assertion wasGeneratedBy ECO_0000203 NP718067.RAbp2e3O3IpEXpECNniQEVmG_TqvrK836dtaB1yPT9F6Q130_provenance.