Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP478688.RActP75OMoDGDE0V0i3IJyPNdk4cmaEgtmPb1gYGKGDik130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP478688.RActP75OMoDGDE0V0i3IJyPNdk4cmaEgtmPb1gYGKGDik130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478688.RActP75OMoDGDE0V0i3IJyPNdk4cmaEgtmPb1gYGKGDik130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478688.RActP75OMoDGDE0V0i3IJyPNdk4cmaEgtmPb1gYGKGDik130_provenance.
- NP478688.RActP75OMoDGDE0V0i3IJyPNdk4cmaEgtmPb1gYGKGDik130_assertion description "[The objective was to compare the contribution to perinatal bilirubinemia of hemolysis and UDP-glucuronosyltransferase (UGT) gene promoter polymorphism, seen in Gilbert's syndrome, between glucose-6-phosphate dehydrogenase (G-6-PD)-deficient and -normal neonates.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478688.RActP75OMoDGDE0V0i3IJyPNdk4cmaEgtmPb1gYGKGDik130_provenance.
- NP478688.RActP75OMoDGDE0V0i3IJyPNdk4cmaEgtmPb1gYGKGDik130_assertion evidence source_evidence_literature NP478688.RActP75OMoDGDE0V0i3IJyPNdk4cmaEgtmPb1gYGKGDik130_provenance.
- NP478688.RActP75OMoDGDE0V0i3IJyPNdk4cmaEgtmPb1gYGKGDik130_assertion SIO_000772 11568299 NP478688.RActP75OMoDGDE0V0i3IJyPNdk4cmaEgtmPb1gYGKGDik130_provenance.
- NP478688.RActP75OMoDGDE0V0i3IJyPNdk4cmaEgtmPb1gYGKGDik130_assertion wasDerivedFrom befree-20140225 NP478688.RActP75OMoDGDE0V0i3IJyPNdk4cmaEgtmPb1gYGKGDik130_provenance.
- NP478688.RActP75OMoDGDE0V0i3IJyPNdk4cmaEgtmPb1gYGKGDik130_assertion wasGeneratedBy ECO_0000203 NP478688.RActP75OMoDGDE0V0i3IJyPNdk4cmaEgtmPb1gYGKGDik130_provenance.
- befree-20140225 importedOn "2014-02-25" NP478688.RActP75OMoDGDE0V0i3IJyPNdk4cmaEgtmPb1gYGKGDik130_provenance.