Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP988503.RADhq8HfzNP1QS8tYTVE8aovFyYO0iLdcOGTj48sHB2dA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP988503.RADhq8HfzNP1QS8tYTVE8aovFyYO0iLdcOGTj48sHB2dA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP988503.RADhq8HfzNP1QS8tYTVE8aovFyYO0iLdcOGTj48sHB2dA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP988503.RADhq8HfzNP1QS8tYTVE8aovFyYO0iLdcOGTj48sHB2dA130_provenance.
- NP988503.RADhq8HfzNP1QS8tYTVE8aovFyYO0iLdcOGTj48sHB2dA130_assertion description "[A statistically significant increase in the frequency of the GST null genotype was observed in male patients who developed myeloid malignancies as compared to male ALL control patients (P = 0.036), but was not observed in female patients (P = 0.51).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988503.RADhq8HfzNP1QS8tYTVE8aovFyYO0iLdcOGTj48sHB2dA130_provenance.
- NP988503.RADhq8HfzNP1QS8tYTVE8aovFyYO0iLdcOGTj48sHB2dA130_assertion evidence source_evidence_literature NP988503.RADhq8HfzNP1QS8tYTVE8aovFyYO0iLdcOGTj48sHB2dA130_provenance.
- NP988503.RADhq8HfzNP1QS8tYTVE8aovFyYO0iLdcOGTj48sHB2dA130_assertion SIO_000772 10673738 NP988503.RADhq8HfzNP1QS8tYTVE8aovFyYO0iLdcOGTj48sHB2dA130_provenance.
- NP988503.RADhq8HfzNP1QS8tYTVE8aovFyYO0iLdcOGTj48sHB2dA130_assertion wasDerivedFrom befree-20150227 NP988503.RADhq8HfzNP1QS8tYTVE8aovFyYO0iLdcOGTj48sHB2dA130_provenance.
- NP988503.RADhq8HfzNP1QS8tYTVE8aovFyYO0iLdcOGTj48sHB2dA130_assertion wasGeneratedBy ECO_0000203 NP988503.RADhq8HfzNP1QS8tYTVE8aovFyYO0iLdcOGTj48sHB2dA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP988503.RADhq8HfzNP1QS8tYTVE8aovFyYO0iLdcOGTj48sHB2dA130_provenance.