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- source_evidence_literature type ECO_0000212 NP104966.RAQ5seLar_faFNvC2Zxtuj84n9p5S8EwcJt6vfaIPSXjA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP104966.RAQ5seLar_faFNvC2Zxtuj84n9p5S8EwcJt6vfaIPSXjA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP104966.RAQ5seLar_faFNvC2Zxtuj84n9p5S8EwcJt6vfaIPSXjA130_provenance.
- NP104966.RAQ5seLar_faFNvC2Zxtuj84n9p5S8EwcJt6vfaIPSXjA130_assertion description "[The homozygous frequency of GSTP1 genotype did not differ significantly between groups of ALL (3.7%), ANLL patients (9.1%) and controls (4.9%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP104966.RAQ5seLar_faFNvC2Zxtuj84n9p5S8EwcJt6vfaIPSXjA130_provenance.
- NP104966.RAQ5seLar_faFNvC2Zxtuj84n9p5S8EwcJt6vfaIPSXjA130_assertion evidence source_evidence_literature NP104966.RAQ5seLar_faFNvC2Zxtuj84n9p5S8EwcJt6vfaIPSXjA130_provenance.
- NP104966.RAQ5seLar_faFNvC2Zxtuj84n9p5S8EwcJt6vfaIPSXjA130_assertion SIO_000772 12827651 NP104966.RAQ5seLar_faFNvC2Zxtuj84n9p5S8EwcJt6vfaIPSXjA130_provenance.
- NP104966.RAQ5seLar_faFNvC2Zxtuj84n9p5S8EwcJt6vfaIPSXjA130_assertion wasDerivedFrom gad-20150221 NP104966.RAQ5seLar_faFNvC2Zxtuj84n9p5S8EwcJt6vfaIPSXjA130_provenance.
- NP104966.RAQ5seLar_faFNvC2Zxtuj84n9p5S8EwcJt6vfaIPSXjA130_assertion wasGeneratedBy ECO_0000203 NP104966.RAQ5seLar_faFNvC2Zxtuj84n9p5S8EwcJt6vfaIPSXjA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP104966.RAQ5seLar_faFNvC2Zxtuj84n9p5S8EwcJt6vfaIPSXjA130_provenance.