Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP495538.RAmC_NNGfcPWVBUWWjZLX7v184mV4NfSItynl6lzNoJfE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP495538.RAmC_NNGfcPWVBUWWjZLX7v184mV4NfSItynl6lzNoJfE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP495538.RAmC_NNGfcPWVBUWWjZLX7v184mV4NfSItynl6lzNoJfE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP495538.RAmC_NNGfcPWVBUWWjZLX7v184mV4NfSItynl6lzNoJfE130_provenance.
- befree-2016 importedOn "2016-02-19" NP495538.RAmC_NNGfcPWVBUWWjZLX7v184mV4NfSItynl6lzNoJfE130_provenance.
- NP495538.RAmC_NNGfcPWVBUWWjZLX7v184mV4NfSItynl6lzNoJfE130_assertion wasGeneratedBy ECO_0000203 NP495538.RAmC_NNGfcPWVBUWWjZLX7v184mV4NfSItynl6lzNoJfE130_provenance.
- NP495538.RAmC_NNGfcPWVBUWWjZLX7v184mV4NfSItynl6lzNoJfE130_assertion wasDerivedFrom befree-2016 NP495538.RAmC_NNGfcPWVBUWWjZLX7v184mV4NfSItynl6lzNoJfE130_provenance.
- NP495538.RAmC_NNGfcPWVBUWWjZLX7v184mV4NfSItynl6lzNoJfE130_assertion SIO_000772 15901999 NP495538.RAmC_NNGfcPWVBUWWjZLX7v184mV4NfSItynl6lzNoJfE130_provenance.
- NP495538.RAmC_NNGfcPWVBUWWjZLX7v184mV4NfSItynl6lzNoJfE130_assertion evidence source_evidence_literature NP495538.RAmC_NNGfcPWVBUWWjZLX7v184mV4NfSItynl6lzNoJfE130_provenance.
- NP495538.RAmC_NNGfcPWVBUWWjZLX7v184mV4NfSItynl6lzNoJfE130_assertion description "[The GST T1 null genotype frequency in CML patients is significantly different from that in controls (odds ratio (OR) 3.12, 95% confidence interval (CI) 1.3-7.45, P=0.008).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP495538.RAmC_NNGfcPWVBUWWjZLX7v184mV4NfSItynl6lzNoJfE130_provenance.