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- NP513269.RAbGGGRidbPbQa8Eg1Ns7nOf98N4512sRWXBNgROvYeSc130_assertion type Assertion NP513269.RAbGGGRidbPbQa8Eg1Ns7nOf98N4512sRWXBNgROvYeSc130_head.
- NP513269.RAbGGGRidbPbQa8Eg1Ns7nOf98N4512sRWXBNgROvYeSc130_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." NP513269.RAbGGGRidbPbQa8Eg1Ns7nOf98N4512sRWXBNgROvYeSc130_provenance.
- NP513269.RAbGGGRidbPbQa8Eg1Ns7nOf98N4512sRWXBNgROvYeSc130_assertion evidence source_evidence_literature NP513269.RAbGGGRidbPbQa8Eg1Ns7nOf98N4512sRWXBNgROvYeSc130_provenance.
- NP513269.RAbGGGRidbPbQa8Eg1Ns7nOf98N4512sRWXBNgROvYeSc130_assertion SIO_000772 12087194 NP513269.RAbGGGRidbPbQa8Eg1Ns7nOf98N4512sRWXBNgROvYeSc130_provenance.
- NP513269.RAbGGGRidbPbQa8Eg1Ns7nOf98N4512sRWXBNgROvYeSc130_assertion wasDerivedFrom befree-20140225 NP513269.RAbGGGRidbPbQa8Eg1Ns7nOf98N4512sRWXBNgROvYeSc130_provenance.
- NP513269.RAbGGGRidbPbQa8Eg1Ns7nOf98N4512sRWXBNgROvYeSc130_assertion wasGeneratedBy ECO_0000203 NP513269.RAbGGGRidbPbQa8Eg1Ns7nOf98N4512sRWXBNgROvYeSc130_provenance.