Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP929229.RAhiTMehHt3BsCcGmHBZ1geykomfN099thUsiwT-rv4tc130_assertion> ?p ?o ?g. }
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- NP929229.RAhiTMehHt3BsCcGmHBZ1geykomfN099thUsiwT-rv4tc130_assertion type Assertion NP929229.RAhiTMehHt3BsCcGmHBZ1geykomfN099thUsiwT-rv4tc130_head.
- NP929229.RAhiTMehHt3BsCcGmHBZ1geykomfN099thUsiwT-rv4tc130_assertion description "[We used a comprehensive haplotype analysis to examine the contribution of the ACC-alpha common genetic variation (allele frequency >5%) to breast cancer in a case-control study (1,588 cases/2,600 controls) nested within the European Prospective Investigation into Cancer and Nutrition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP929229.RAhiTMehHt3BsCcGmHBZ1geykomfN099thUsiwT-rv4tc130_provenance.
- NP929229.RAhiTMehHt3BsCcGmHBZ1geykomfN099thUsiwT-rv4tc130_assertion evidence source_evidence_literature NP929229.RAhiTMehHt3BsCcGmHBZ1geykomfN099thUsiwT-rv4tc130_provenance.
- NP929229.RAhiTMehHt3BsCcGmHBZ1geykomfN099thUsiwT-rv4tc130_assertion SIO_000772 17372234 NP929229.RAhiTMehHt3BsCcGmHBZ1geykomfN099thUsiwT-rv4tc130_provenance.
- NP929229.RAhiTMehHt3BsCcGmHBZ1geykomfN099thUsiwT-rv4tc130_assertion wasDerivedFrom befree-20140225 NP929229.RAhiTMehHt3BsCcGmHBZ1geykomfN099thUsiwT-rv4tc130_provenance.
- NP929229.RAhiTMehHt3BsCcGmHBZ1geykomfN099thUsiwT-rv4tc130_assertion wasGeneratedBy ECO_0000203 NP929229.RAhiTMehHt3BsCcGmHBZ1geykomfN099thUsiwT-rv4tc130_provenance.