Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP714088.RAEy08eseb_-CMVQxdOwUgOWitl_-rmSMDsBQAJ8ojKLU130_assertion> ?p ?o ?g. }
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- NP714088.RAEy08eseb_-CMVQxdOwUgOWitl_-rmSMDsBQAJ8ojKLU130_assertion type Assertion NP714088.RAEy08eseb_-CMVQxdOwUgOWitl_-rmSMDsBQAJ8ojKLU130_head.
- NP714088.RAEy08eseb_-CMVQxdOwUgOWitl_-rmSMDsBQAJ8ojKLU130_assertion description "[Crigler-Najjar syndrome type 1 (CN type 1) is an autosomal recessive disorder characterized by nonhemolytic jaundice resulting from mutations to the gene encoding bilirubin-UDP-glucuronosyltransferase (UDPGT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP714088.RAEy08eseb_-CMVQxdOwUgOWitl_-rmSMDsBQAJ8ojKLU130_provenance.
- NP714088.RAEy08eseb_-CMVQxdOwUgOWitl_-rmSMDsBQAJ8ojKLU130_assertion evidence source_evidence_literature NP714088.RAEy08eseb_-CMVQxdOwUgOWitl_-rmSMDsBQAJ8ojKLU130_provenance.
- NP714088.RAEy08eseb_-CMVQxdOwUgOWitl_-rmSMDsBQAJ8ojKLU130_assertion SIO_000772 9525311 NP714088.RAEy08eseb_-CMVQxdOwUgOWitl_-rmSMDsBQAJ8ojKLU130_provenance.
- NP714088.RAEy08eseb_-CMVQxdOwUgOWitl_-rmSMDsBQAJ8ojKLU130_assertion wasDerivedFrom befree-20140225 NP714088.RAEy08eseb_-CMVQxdOwUgOWitl_-rmSMDsBQAJ8ojKLU130_provenance.
- NP714088.RAEy08eseb_-CMVQxdOwUgOWitl_-rmSMDsBQAJ8ojKLU130_assertion wasGeneratedBy ECO_0000203 NP714088.RAEy08eseb_-CMVQxdOwUgOWitl_-rmSMDsBQAJ8ojKLU130_provenance.