Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP122771.RAUhQoJ5IeKnX1mAicxGzykG2RgfASbRHZbqoqXZkmwlU130_assertion> ?p ?o ?g. }
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- NP122771.RAUhQoJ5IeKnX1mAicxGzykG2RgfASbRHZbqoqXZkmwlU130_assertion type Assertion NP122771.RAUhQoJ5IeKnX1mAicxGzykG2RgfASbRHZbqoqXZkmwlU130_head.
- NP122771.RAUhQoJ5IeKnX1mAicxGzykG2RgfASbRHZbqoqXZkmwlU130_assertion description "[Although none of the tested gene polymorphisms was significantly related to an increased risk of COPD alone, our results suggest that the homozygous exon 3 mutant variant of EPHX1 gene in the combination with GSTM1 null genotype is a significant predictor]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP122771.RAUhQoJ5IeKnX1mAicxGzykG2RgfASbRHZbqoqXZkmwlU130_provenance.
- NP122771.RAUhQoJ5IeKnX1mAicxGzykG2RgfASbRHZbqoqXZkmwlU130_assertion evidence source_evidence_literature NP122771.RAUhQoJ5IeKnX1mAicxGzykG2RgfASbRHZbqoqXZkmwlU130_provenance.
- NP122771.RAUhQoJ5IeKnX1mAicxGzykG2RgfASbRHZbqoqXZkmwlU130_assertion SIO_000772 18461673 NP122771.RAUhQoJ5IeKnX1mAicxGzykG2RgfASbRHZbqoqXZkmwlU130_provenance.
- NP122771.RAUhQoJ5IeKnX1mAicxGzykG2RgfASbRHZbqoqXZkmwlU130_assertion wasDerivedFrom gad-20150221 NP122771.RAUhQoJ5IeKnX1mAicxGzykG2RgfASbRHZbqoqXZkmwlU130_provenance.
- NP122771.RAUhQoJ5IeKnX1mAicxGzykG2RgfASbRHZbqoqXZkmwlU130_assertion wasGeneratedBy ECO_0000203 NP122771.RAUhQoJ5IeKnX1mAicxGzykG2RgfASbRHZbqoqXZkmwlU130_provenance.