Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP114163.RAk09O52jBPdeGsc0CG_HGrVgB1EXUdbsDMkEgJ5IbNJE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP114163.RAk09O52jBPdeGsc0CG_HGrVgB1EXUdbsDMkEgJ5IbNJE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP114163.RAk09O52jBPdeGsc0CG_HGrVgB1EXUdbsDMkEgJ5IbNJE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP114163.RAk09O52jBPdeGsc0CG_HGrVgB1EXUdbsDMkEgJ5IbNJE130_provenance.
- NP114163.RAk09O52jBPdeGsc0CG_HGrVgB1EXUdbsDMkEgJ5IbNJE130_assertion description "[For GSTM1 genotypes, the overall values (controls plus patients with thyroid cancer; no.= 335) indicated that the frequency of the null genotype was 49.85%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP114163.RAk09O52jBPdeGsc0CG_HGrVgB1EXUdbsDMkEgJ5IbNJE130_provenance.
- NP114163.RAk09O52jBPdeGsc0CG_HGrVgB1EXUdbsDMkEgJ5IbNJE130_assertion evidence source_evidence_literature NP114163.RAk09O52jBPdeGsc0CG_HGrVgB1EXUdbsDMkEgJ5IbNJE130_provenance.
- NP114163.RAk09O52jBPdeGsc0CG_HGrVgB1EXUdbsDMkEgJ5IbNJE130_assertion SIO_000772 19169061 NP114163.RAk09O52jBPdeGsc0CG_HGrVgB1EXUdbsDMkEgJ5IbNJE130_provenance.
- NP114163.RAk09O52jBPdeGsc0CG_HGrVgB1EXUdbsDMkEgJ5IbNJE130_assertion wasDerivedFrom lhgdn-20090331 NP114163.RAk09O52jBPdeGsc0CG_HGrVgB1EXUdbsDMkEgJ5IbNJE130_provenance.
- NP114163.RAk09O52jBPdeGsc0CG_HGrVgB1EXUdbsDMkEgJ5IbNJE130_assertion wasGeneratedBy ECO_0000203 NP114163.RAk09O52jBPdeGsc0CG_HGrVgB1EXUdbsDMkEgJ5IbNJE130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP114163.RAk09O52jBPdeGsc0CG_HGrVgB1EXUdbsDMkEgJ5IbNJE130_provenance.