Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP689827.RAPEFU1LGD20TWiNcSXG7at14uUFHZOW5WrKdOVIAQbOo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP689827.RAPEFU1LGD20TWiNcSXG7at14uUFHZOW5WrKdOVIAQbOo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP689827.RAPEFU1LGD20TWiNcSXG7at14uUFHZOW5WrKdOVIAQbOo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP689827.RAPEFU1LGD20TWiNcSXG7at14uUFHZOW5WrKdOVIAQbOo130_provenance.
- NP689827.RAPEFU1LGD20TWiNcSXG7at14uUFHZOW5WrKdOVIAQbOo130_assertion description "[Since, we observed a higher incidence of a single nucleotide polymorphism (SNP) at the -25 position in the 5'untranslated region (5'UTR-25) of RPH3AL, we performed the genotyping analysis of this SNP in a retrospective CRC cohort (n=134) to assess their clinical importance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP689827.RAPEFU1LGD20TWiNcSXG7at14uUFHZOW5WrKdOVIAQbOo130_provenance.
- NP689827.RAPEFU1LGD20TWiNcSXG7at14uUFHZOW5WrKdOVIAQbOo130_assertion evidence source_evidence_literature NP689827.RAPEFU1LGD20TWiNcSXG7at14uUFHZOW5WrKdOVIAQbOo130_provenance.
- NP689827.RAPEFU1LGD20TWiNcSXG7at14uUFHZOW5WrKdOVIAQbOo130_assertion SIO_000772 17981610 NP689827.RAPEFU1LGD20TWiNcSXG7at14uUFHZOW5WrKdOVIAQbOo130_provenance.
- NP689827.RAPEFU1LGD20TWiNcSXG7at14uUFHZOW5WrKdOVIAQbOo130_assertion wasDerivedFrom befree-20140225 NP689827.RAPEFU1LGD20TWiNcSXG7at14uUFHZOW5WrKdOVIAQbOo130_provenance.
- NP689827.RAPEFU1LGD20TWiNcSXG7at14uUFHZOW5WrKdOVIAQbOo130_assertion wasGeneratedBy ECO_0000203 NP689827.RAPEFU1LGD20TWiNcSXG7at14uUFHZOW5WrKdOVIAQbOo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP689827.RAPEFU1LGD20TWiNcSXG7at14uUFHZOW5WrKdOVIAQbOo130_provenance.