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- source_evidence_literature type ECO_0000212 NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_provenance.
- NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_assertion description "[? The UGT1A1 211G>A mutation is associated with neonatal hyperbilirubinemia in Asians, but not in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_provenance.
- NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_assertion evidence source_evidence_literature NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_provenance.
- NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_assertion SIO_000772 21272068 NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_provenance.
- NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_assertion wasDerivedFrom befree-2016 NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_provenance.
- NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_assertion wasGeneratedBy ECO_0000203 NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_provenance.
- befree-2016 importedOn "2016-02-19" NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_provenance.