Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP274943.RA7Pv_wWLFLcxXQR_MBV0IdBUFIWmHOKw0r-rD-ALxoB0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP274943.RA7Pv_wWLFLcxXQR_MBV0IdBUFIWmHOKw0r-rD-ALxoB0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP274943.RA7Pv_wWLFLcxXQR_MBV0IdBUFIWmHOKw0r-rD-ALxoB0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP274943.RA7Pv_wWLFLcxXQR_MBV0IdBUFIWmHOKw0r-rD-ALxoB0130_provenance.
- NP274943.RA7Pv_wWLFLcxXQR_MBV0IdBUFIWmHOKw0r-rD-ALxoB0130_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." NP274943.RA7Pv_wWLFLcxXQR_MBV0IdBUFIWmHOKw0r-rD-ALxoB0130_provenance.
- NP274943.RA7Pv_wWLFLcxXQR_MBV0IdBUFIWmHOKw0r-rD-ALxoB0130_assertion evidence source_evidence_literature NP274943.RA7Pv_wWLFLcxXQR_MBV0IdBUFIWmHOKw0r-rD-ALxoB0130_provenance.
- NP274943.RA7Pv_wWLFLcxXQR_MBV0IdBUFIWmHOKw0r-rD-ALxoB0130_assertion SIO_000772 10673738 NP274943.RA7Pv_wWLFLcxXQR_MBV0IdBUFIWmHOKw0r-rD-ALxoB0130_provenance.
- NP274943.RA7Pv_wWLFLcxXQR_MBV0IdBUFIWmHOKw0r-rD-ALxoB0130_assertion wasDerivedFrom befree-2016 NP274943.RA7Pv_wWLFLcxXQR_MBV0IdBUFIWmHOKw0r-rD-ALxoB0130_provenance.
- NP274943.RA7Pv_wWLFLcxXQR_MBV0IdBUFIWmHOKw0r-rD-ALxoB0130_assertion wasGeneratedBy ECO_0000203 NP274943.RA7Pv_wWLFLcxXQR_MBV0IdBUFIWmHOKw0r-rD-ALxoB0130_provenance.
- befree-2016 importedOn "2016-02-19" NP274943.RA7Pv_wWLFLcxXQR_MBV0IdBUFIWmHOKw0r-rD-ALxoB0130_provenance.