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- NP883625.RAH4DfBzvU34_YSi3xrwEtHl3FStczsLHJ2SJSCg1FnS0130_assertion type Assertion NP883625.RAH4DfBzvU34_YSi3xrwEtHl3FStczsLHJ2SJSCg1FnS0130_head.
- NP883625.RAH4DfBzvU34_YSi3xrwEtHl3FStczsLHJ2SJSCg1FnS0130_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." NP883625.RAH4DfBzvU34_YSi3xrwEtHl3FStczsLHJ2SJSCg1FnS0130_provenance.
- NP883625.RAH4DfBzvU34_YSi3xrwEtHl3FStczsLHJ2SJSCg1FnS0130_assertion evidence source_evidence_literature NP883625.RAH4DfBzvU34_YSi3xrwEtHl3FStczsLHJ2SJSCg1FnS0130_provenance.
- NP883625.RAH4DfBzvU34_YSi3xrwEtHl3FStczsLHJ2SJSCg1FnS0130_assertion SIO_000772 9525311 NP883625.RAH4DfBzvU34_YSi3xrwEtHl3FStczsLHJ2SJSCg1FnS0130_provenance.
- NP883625.RAH4DfBzvU34_YSi3xrwEtHl3FStczsLHJ2SJSCg1FnS0130_assertion wasDerivedFrom befree-20140225 NP883625.RAH4DfBzvU34_YSi3xrwEtHl3FStczsLHJ2SJSCg1FnS0130_provenance.
- NP883625.RAH4DfBzvU34_YSi3xrwEtHl3FStczsLHJ2SJSCg1FnS0130_assertion wasGeneratedBy ECO_0000203 NP883625.RAH4DfBzvU34_YSi3xrwEtHl3FStczsLHJ2SJSCg1FnS0130_provenance.