Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP369427.RAm11erTVzBbiPOH4eP4b4ZLdBLdVyPn8ZbT4Pbrk00FU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP369427.RAm11erTVzBbiPOH4eP4b4ZLdBLdVyPn8ZbT4Pbrk00FU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP369427.RAm11erTVzBbiPOH4eP4b4ZLdBLdVyPn8ZbT4Pbrk00FU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP369427.RAm11erTVzBbiPOH4eP4b4ZLdBLdVyPn8ZbT4Pbrk00FU130_provenance.
- NP369427.RAm11erTVzBbiPOH4eP4b4ZLdBLdVyPn8ZbT4Pbrk00FU130_assertion description "[In conclusion, this study has demonstrated that variation at nucleotide 211 of the UGT1A1 gene is a risk factor for the development of neonatal hyperbilirubinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP369427.RAm11erTVzBbiPOH4eP4b4ZLdBLdVyPn8ZbT4Pbrk00FU130_provenance.
- NP369427.RAm11erTVzBbiPOH4eP4b4ZLdBLdVyPn8ZbT4Pbrk00FU130_assertion evidence source_evidence_literature NP369427.RAm11erTVzBbiPOH4eP4b4ZLdBLdVyPn8ZbT4Pbrk00FU130_provenance.
- NP369427.RAm11erTVzBbiPOH4eP4b4ZLdBLdVyPn8ZbT4Pbrk00FU130_assertion SIO_000772 12357057 NP369427.RAm11erTVzBbiPOH4eP4b4ZLdBLdVyPn8ZbT4Pbrk00FU130_provenance.
- NP369427.RAm11erTVzBbiPOH4eP4b4ZLdBLdVyPn8ZbT4Pbrk00FU130_assertion wasDerivedFrom befree-2016 NP369427.RAm11erTVzBbiPOH4eP4b4ZLdBLdVyPn8ZbT4Pbrk00FU130_provenance.
- NP369427.RAm11erTVzBbiPOH4eP4b4ZLdBLdVyPn8ZbT4Pbrk00FU130_assertion wasGeneratedBy ECO_0000203 NP369427.RAm11erTVzBbiPOH4eP4b4ZLdBLdVyPn8ZbT4Pbrk00FU130_provenance.
- befree-2016 importedOn "2016-02-19" NP369427.RAm11erTVzBbiPOH4eP4b4ZLdBLdVyPn8ZbT4Pbrk00FU130_provenance.