Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Although there was little statistical power to detect modest increases in risk for the homozygote variant genotypes, particularly for the rare RAD51 and XRCC2 variants, the data suggest that none of these variants play a major role in the etiology of breast or ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP875193.RAZ84hEZrJrCe0JIjzzTEnHw7XAWNs_dflKbn1U-jiJ9E130_assertion description "[Although there was little statistical power to detect modest increases in risk for the homozygote variant genotypes, particularly for the rare RAD51 and XRCC2 variants, the data suggest that none of these variants play a major role in the etiology of breast or ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP875193.RAZ84hEZrJrCe0JIjzzTEnHw7XAWNs_dflKbn1U-jiJ9E130_provenance.
• assertion description "[Although there was little statistical power to detect modest increases in risk for the homozygote variant genotypes, particularly for the rare RAD51 and XRCC2 variants, the data suggest that none of these variants play a major role in the etiology of breast or ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Although there was little statistical power to detect modest increases in risk for the homozygote variant genotypes, particularly for the rare RAD51 and XRCC2 variants, the data suggest that none of these variants play a major role in the etiology of breast or ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Although there was little statistical power to detect modest increases in risk for the homozygote variant genotypes, particularly for the rare RAD51 and XRCC2 variants, the data suggest that none of these variants play a major role in the etiology of breast or ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Although there was little statistical power to detect modest increases in risk for the homozygote variant genotypes, particularly for the rare RAD51 and XRCC2 variants, the data suggest that none of these variants play a major role in the etiology of breast or ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP780447.RAv-lLxrtSotKGQRJZhDnq1yaT9s0CU3fCVzTAlGlL0Wg130_assertion description "[Although there was little statistical power to detect modest increases in risk for the homozygote variant genotypes, particularly for the rare RAD51 and XRCC2 variants, the data suggest that none of these variants play a major role in the etiology of breast or ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP780447.RAv-lLxrtSotKGQRJZhDnq1yaT9s0CU3fCVzTAlGlL0Wg130_provenance.
• NP482655.RATpZrkFWzyg6HyonFiZy68wj_AheDixML7RLv-4jjeso130_assertion description "[Although there was little statistical power to detect modest increases in risk for the homozygote variant genotypes, particularly for the rare RAD51 and XRCC2 variants, the data suggest that none of these variants play a major role in the etiology of breast or ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP482655.RATpZrkFWzyg6HyonFiZy68wj_AheDixML7RLv-4jjeso130_provenance.
• NP482660.RAu5LzmKDcSx9QFLJ1_I3N5d2HaJ4NwVWO2uBJF2h8BjQ130_assertion description "[Although there was little statistical power to detect modest increases in risk for the homozygote variant genotypes, particularly for the rare RAD51 and XRCC2 variants, the data suggest that none of these variants play a major role in the etiology of breast or ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP482660.RAu5LzmKDcSx9QFLJ1_I3N5d2HaJ4NwVWO2uBJF2h8BjQ130_provenance.
• NP482664.RAvmheSY_rh5Xx5W4ughRKojkyKwbIKsG8g0RIXneZD3s130_assertion description "[Although there was little statistical power to detect modest increases in risk for the homozygote variant genotypes, particularly for the rare RAD51 and XRCC2 variants, the data suggest that none of these variants play a major role in the etiology of breast or ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP482664.RAvmheSY_rh5Xx5W4ughRKojkyKwbIKsG8g0RIXneZD3s130_provenance.
• NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_assertion description "[Although there was little statistical power to detect modest increases in risk for the homozygote variant genotypes, particularly for the rare RAD51 and XRCC2 variants, the data suggest that none of these variants play a major role in the etiology of breast or ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_provenance.
• NP482657.RAHH2vco7dJKBgyX9z3HbG9lyC9hKC4Edq4KDrSxfHF8U130_assertion description "[Although there was little statistical power to detect modest increases in risk for the homozygote variant genotypes, particularly for the rare RAD51 and XRCC2 variants, the data suggest that none of these variants play a major role in the etiology of breast or ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP482657.RAHH2vco7dJKBgyX9z3HbG9lyC9hKC4Edq4KDrSxfHF8U130_provenance.