Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[This chapter focuses on recent genome-wide studies that have utilized high-density single nucleotide polymorphism (SNP) genotyping arrays to discover genetic factors predisposing to tumor initiation such as rare mutations at locus 2p23 (in ALK gene) for familial neuroblastoma, common SNPs at 6p22 (FLJ22536 and FLJ44180) and 2q35 (BARD1), and a copy number polymorphism at 1q21.1 (NBPF23) for sporadic neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• assertion description "[This chapter focuses on recent genome-wide studies that have utilized high-density single nucleotide polymorphism (SNP) genotyping arrays to discover genetic factors predisposing to tumor initiation such as rare mutations at locus 2p23 (in ALK gene) for familial neuroblastoma, common SNPs at 6p22 (FLJ22536 and FLJ44180) and 2q35 (BARD1), and a copy number polymorphism at 1q21.1 (NBPF23) for sporadic neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP822466.RAaXSStQ04R32iqQIi2qIvNvy5--ZV5CrDl2bF9Wrd1wg130_assertion description "[This chapter focuses on recent genome-wide studies that have utilized high-density single nucleotide polymorphism (SNP) genotyping arrays to discover genetic factors predisposing to tumor initiation such as rare mutations at locus 2p23 (in ALK gene) for familial neuroblastoma, common SNPs at 6p22 (FLJ22536 and FLJ44180) and 2q35 (BARD1), and a copy number polymorphism at 1q21.1 (NBPF23) for sporadic neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP822466.RAaXSStQ04R32iqQIi2qIvNvy5--ZV5CrDl2bF9Wrd1wg130_provenance.
• NP313717.RAdj20Oo0LOLEoH6xW-b1oyhAzlgrKUylQfGLlMjZsN6w130_assertion description "[This chapter focuses on recent genome-wide studies that have utilized high-density single nucleotide polymorphism (SNP) genotyping arrays to discover genetic factors predisposing to tumor initiation such as rare mutations at locus 2p23 (in ALK gene) for familial neuroblastoma, common SNPs at 6p22 (FLJ22536 and FLJ44180) and 2q35 (BARD1), and a copy number polymorphism at 1q21.1 (NBPF23) for sporadic neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP313717.RAdj20Oo0LOLEoH6xW-b1oyhAzlgrKUylQfGLlMjZsN6w130_provenance.
• NP569180.RA7erUhOCVGX1mNwQlecOsMFGoRwCMJ-xHJwpZViXRYq8130_assertion description "[This chapter focuses on recent genome-wide studies that have utilized high-density single nucleotide polymorphism (SNP) genotyping arrays to discover genetic factors predisposing to tumor initiation such as rare mutations at locus 2p23 (in ALK gene) for familial neuroblastoma, common SNPs at 6p22 (FLJ22536 and FLJ44180) and 2q35 (BARD1), and a copy number polymorphism at 1q21.1 (NBPF23) for sporadic neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569180.RA7erUhOCVGX1mNwQlecOsMFGoRwCMJ-xHJwpZViXRYq8130_provenance.
• assertion description "[This chapter focuses on recent genome-wide studies that have utilized high-density single nucleotide polymorphism (SNP) genotyping arrays to discover genetic factors predisposing to tumor initiation such as rare mutations at locus 2p23 (in ALK gene) for familial neuroblastoma, common SNPs at 6p22 (FLJ22536 and FLJ44180) and 2q35 (BARD1), and a copy number polymorphism at 1q21.1 (NBPF23) for sporadic neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP699581.RA7R1lLUIZpBqDW_rRx-TfKy6p_sQez4xEnzEWI8UX43A130_assertion description "[This chapter focuses on recent genome-wide studies that have utilized high-density single nucleotide polymorphism (SNP) genotyping arrays to discover genetic factors predisposing to tumor initiation such as rare mutations at locus 2p23 (in ALK gene) for familial neuroblastoma, common SNPs at 6p22 (FLJ22536 and FLJ44180) and 2q35 (BARD1), and a copy number polymorphism at 1q21.1 (NBPF23) for sporadic neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP699581.RA7R1lLUIZpBqDW_rRx-TfKy6p_sQez4xEnzEWI8UX43A130_provenance.
• NP587819.RAK-I2dYDakFNeRL9UHkXv8_aIKPxJUI2XGhE7Of4mTTU130_assertion description "[This chapter focuses on recent genome-wide studies that have utilized high-density single nucleotide polymorphism (SNP) genotyping arrays to discover genetic factors predisposing to tumor initiation such as rare mutations at locus 2p23 (in ALK gene) for familial neuroblastoma, common SNPs at 6p22 (FLJ22536 and FLJ44180) and 2q35 (BARD1), and a copy number polymorphism at 1q21.1 (NBPF23) for sporadic neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587819.RAK-I2dYDakFNeRL9UHkXv8_aIKPxJUI2XGhE7Of4mTTU130_provenance.
• NP991583.RAaeYkghgODqwZBluS1ZnJjri0IZeWvtBFPpf72XVr5pU130_assertion description "[This chapter focuses on recent genome-wide studies that have utilized high-density single nucleotide polymorphism (SNP) genotyping arrays to discover genetic factors predisposing to tumor initiation such as rare mutations at locus 2p23 (in ALK gene) for familial neuroblastoma, common SNPs at 6p22 (FLJ22536 and FLJ44180) and 2q35 (BARD1), and a copy number polymorphism at 1q21.1 (NBPF23) for sporadic neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP991583.RAaeYkghgODqwZBluS1ZnJjri0IZeWvtBFPpf72XVr5pU130_provenance.
• NP259186.RAl14s_C_hn95N-E6L2HMbQDWjZv3Sra7vHOGDGBm8yHU130_assertion description "[This chapter focuses on recent genome-wide studies that have utilized high-density single nucleotide polymorphism (SNP) genotyping arrays to discover genetic factors predisposing to tumor initiation such as rare mutations at locus 2p23 (in ALK gene) for familial neuroblastoma, common SNPs at 6p22 (FLJ22536 and FLJ44180) and 2q35 (BARD1), and a copy number polymorphism at 1q21.1 (NBPF23) for sporadic neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP259186.RAl14s_C_hn95N-E6L2HMbQDWjZv3Sra7vHOGDGBm8yHU130_provenance.
• NP259221.RAmn074AjUT0wFHytpx-xxyYul5oARsy0aLsuPn53NVME130_assertion description "[This chapter focuses on recent genome-wide studies that have utilized high-density single nucleotide polymorphism (SNP) genotyping arrays to discover genetic factors predisposing to tumor initiation such as rare mutations at locus 2p23 (in ALK gene) for familial neuroblastoma, common SNPs at 6p22 (FLJ22536 and FLJ44180) and 2q35 (BARD1), and a copy number polymorphism at 1q21.1 (NBPF23) for sporadic neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP259221.RAmn074AjUT0wFHytpx-xxyYul5oARsy0aLsuPn53NVME130_provenance.
• NP816098.RAAcaHTPioxk23KG0_ooazfb3AA9RMoBQBqHVOJoK2U3k130_assertion description "[This chapter focuses on recent genome-wide studies that have utilized high-density single nucleotide polymorphism (SNP) genotyping arrays to discover genetic factors predisposing to tumor initiation such as rare mutations at locus 2p23 (in ALK gene) for familial neuroblastoma, common SNPs at 6p22 (FLJ22536 and FLJ44180) and 2q35 (BARD1), and a copy number polymorphism at 1q21.1 (NBPF23) for sporadic neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP816098.RAAcaHTPioxk23KG0_ooazfb3AA9RMoBQBqHVOJoK2U3k130_provenance.
• NP816101.RAcQ1-5Cj1vPMXNZstV_VeIGPlfyIRHwbAsW1n0SYmr48130_assertion description "[This chapter focuses on recent genome-wide studies that have utilized high-density single nucleotide polymorphism (SNP) genotyping arrays to discover genetic factors predisposing to tumor initiation such as rare mutations at locus 2p23 (in ALK gene) for familial neuroblastoma, common SNPs at 6p22 (FLJ22536 and FLJ44180) and 2q35 (BARD1), and a copy number polymorphism at 1q21.1 (NBPF23) for sporadic neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP816101.RAcQ1-5Cj1vPMXNZstV_VeIGPlfyIRHwbAsW1n0SYmr48130_provenance.
• NP991585.RAisCzNfGR6OLlv1dY7KEzdELRSPwegpJm8f3PI7qszB0130_assertion description "[This chapter focuses on recent genome-wide studies that have utilized high-density single nucleotide polymorphism (SNP) genotyping arrays to discover genetic factors predisposing to tumor initiation such as rare mutations at locus 2p23 (in ALK gene) for familial neuroblastoma, common SNPs at 6p22 (FLJ22536 and FLJ44180) and 2q35 (BARD1), and a copy number polymorphism at 1q21.1 (NBPF23) for sporadic neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP991585.RAisCzNfGR6OLlv1dY7KEzdELRSPwegpJm8f3PI7qszB0130_provenance.
• NP816099.RAhh_IGwvnW7U8robjABmpsxLX_G7neh4zmbLK3u5yFFY130_assertion description "[This chapter focuses on recent genome-wide studies that have utilized high-density single nucleotide polymorphism (SNP) genotyping arrays to discover genetic factors predisposing to tumor initiation such as rare mutations at locus 2p23 (in ALK gene) for familial neuroblastoma, common SNPs at 6p22 (FLJ22536 and FLJ44180) and 2q35 (BARD1), and a copy number polymorphism at 1q21.1 (NBPF23) for sporadic neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP816099.RAhh_IGwvnW7U8robjABmpsxLX_G7neh4zmbLK3u5yFFY130_provenance.
• NP816100.RAvaczI3arEJOHIY7z1KPqxo1o8gmm889BggRo49Ae8hA130_assertion description "[This chapter focuses on recent genome-wide studies that have utilized high-density single nucleotide polymorphism (SNP) genotyping arrays to discover genetic factors predisposing to tumor initiation such as rare mutations at locus 2p23 (in ALK gene) for familial neuroblastoma, common SNPs at 6p22 (FLJ22536 and FLJ44180) and 2q35 (BARD1), and a copy number polymorphism at 1q21.1 (NBPF23) for sporadic neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP816100.RAvaczI3arEJOHIY7z1KPqxo1o8gmm889BggRo49Ae8hA130_provenance.
• NP259236.RAweFmXizUma54AbZlzwO1TUOKFluQnBGrEkhIKzE_fyQ130_assertion description "[This chapter focuses on recent genome-wide studies that have utilized high-density single nucleotide polymorphism (SNP) genotyping arrays to discover genetic factors predisposing to tumor initiation such as rare mutations at locus 2p23 (in ALK gene) for familial neuroblastoma, common SNPs at 6p22 (FLJ22536 and FLJ44180) and 2q35 (BARD1), and a copy number polymorphism at 1q21.1 (NBPF23) for sporadic neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP259236.RAweFmXizUma54AbZlzwO1TUOKFluQnBGrEkhIKzE_fyQ130_provenance.
• NP816096.RANZTaQFNzQwBUZuFGBVMHXCZKKd8q4F7P2FsbBLGt43M130_assertion description "[This chapter focuses on recent genome-wide studies that have utilized high-density single nucleotide polymorphism (SNP) genotyping arrays to discover genetic factors predisposing to tumor initiation such as rare mutations at locus 2p23 (in ALK gene) for familial neuroblastoma, common SNPs at 6p22 (FLJ22536 and FLJ44180) and 2q35 (BARD1), and a copy number polymorphism at 1q21.1 (NBPF23) for sporadic neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP816096.RANZTaQFNzQwBUZuFGBVMHXCZKKd8q4F7P2FsbBLGt43M130_provenance.
• NP816095.RAzOfmhuTQm46iDTgeCOUfCMIo1hdek52fbfQx3kM61cQ130_assertion description "[This chapter focuses on recent genome-wide studies that have utilized high-density single nucleotide polymorphism (SNP) genotyping arrays to discover genetic factors predisposing to tumor initiation such as rare mutations at locus 2p23 (in ALK gene) for familial neuroblastoma, common SNPs at 6p22 (FLJ22536 and FLJ44180) and 2q35 (BARD1), and a copy number polymorphism at 1q21.1 (NBPF23) for sporadic neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP816095.RAzOfmhuTQm46iDTgeCOUfCMIo1hdek52fbfQx3kM61cQ130_provenance.
• NP816097.RAyPm1_ZECfYHdTphGPymq0t870z7XPccydNCeGy_SukI130_assertion description "[This chapter focuses on recent genome-wide studies that have utilized high-density single nucleotide polymorphism (SNP) genotyping arrays to discover genetic factors predisposing to tumor initiation such as rare mutations at locus 2p23 (in ALK gene) for familial neuroblastoma, common SNPs at 6p22 (FLJ22536 and FLJ44180) and 2q35 (BARD1), and a copy number polymorphism at 1q21.1 (NBPF23) for sporadic neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP816097.RAyPm1_ZECfYHdTphGPymq0t870z7XPccydNCeGy_SukI130_provenance.