Matches in Nanopublications for { ?s ?p "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP565904.RAT1AMiA4O3NmvObQT-442lzdTqO1gBhdZmXRDy10pad8130_assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP565904.RAT1AMiA4O3NmvObQT-442lzdTqO1gBhdZmXRDy10pad8130_provenance.
- NP812852.RAVnWQZUqiaAkA4iJ92cgVwmFoPwusIQk_xVq2NgIglIg130_assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP812852.RAVnWQZUqiaAkA4iJ92cgVwmFoPwusIQk_xVq2NgIglIg130_provenance.
- assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP374097.RAXC6Jwbn2DO-iNVFzQ1s3r6lhKOV2y4ZmMOSUcvWmxM8130_assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374097.RAXC6Jwbn2DO-iNVFzQ1s3r6lhKOV2y4ZmMOSUcvWmxM8130_provenance.
- NP84828.RASmWuKEDsnbrOaoUGmNMefSyoZYyzH7wIMOs2yqmUSFs130_assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP84828.RASmWuKEDsnbrOaoUGmNMefSyoZYyzH7wIMOs2yqmUSFs130_provenance.
- NP532034.RARNRKmHWk_B6UWNH7NJ4KfGh_Ietcx4BYqpEIa3pHKUQ130_assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532034.RARNRKmHWk_B6UWNH7NJ4KfGh_Ietcx4BYqpEIa3pHKUQ130_provenance.
- NP7557.RAQiS9_QuWyPVRTDThv3copI5DQDArfwnre2jAYQ9o-h8130_assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7557.RAQiS9_QuWyPVRTDThv3copI5DQDArfwnre2jAYQ9o-h8130_provenance.
- NP20731.RAwHHyeGRp31isiFGZU5MEunI4yFcVZZI6Ye7hidwKkPk130_assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20731.RAwHHyeGRp31isiFGZU5MEunI4yFcVZZI6Ye7hidwKkPk130_provenance.
- assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_provenance.
- NP600336.RAAi70XkRM6XF3oOaGXpKboe-bLLs2Z1l2J5tga-bvcLQ130_assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600336.RAAi70XkRM6XF3oOaGXpKboe-bLLs2Z1l2J5tga-bvcLQ130_provenance.
- NP23342.RAH5JDR97V085d8Si6q-n9JZLAgKCHFJHWCv_fMnrvjQQ130_assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP23342.RAH5JDR97V085d8Si6q-n9JZLAgKCHFJHWCv_fMnrvjQQ130_provenance.
- NP106284.RAgRRJKWPpXurl7UHx1kRZJLDnGxgabWAZO7HMX8-R3R8130_assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP106284.RAgRRJKWPpXurl7UHx1kRZJLDnGxgabWAZO7HMX8-R3R8130_provenance.
- NP106285.RAmHF9Qn3OtOAFScMM7XZ3eRWSlb9T-iSkZuh2H-zqNQ4130_assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP106285.RAmHF9Qn3OtOAFScMM7XZ3eRWSlb9T-iSkZuh2H-zqNQ4130_provenance.
- NP600337.RAj0cMLtO1aAHx1gEgND4LoNgqM1sWQYVn366Wzq1bc7c130_assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600337.RAj0cMLtO1aAHx1gEgND4LoNgqM1sWQYVn366Wzq1bc7c130_provenance.
- NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_provenance.
- NP220495.RAIRYwhFuJ5f5COiCFNoZSGqP8PstdIpEAo1WHYXCk4zs130_assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220495.RAIRYwhFuJ5f5COiCFNoZSGqP8PstdIpEAo1WHYXCk4zs130_provenance.
- NP106286.RAHOR2w6DqijNRyS1Iga8uxjyVSjcsgwBQhmiiLChIFfU130_assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP106286.RAHOR2w6DqijNRyS1Iga8uxjyVSjcsgwBQhmiiLChIFfU130_provenance.
- NP583991.RA6UOtuHl3bkIkeh7l_Wh7B-1SbVHDcpPPJP9z_RgQr7Y130_assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583991.RA6UOtuHl3bkIkeh7l_Wh7B-1SbVHDcpPPJP9z_RgQr7Y130_provenance.
- NP600335.RAOEYH4y96hZQcEpSjL3yKryrihXJZWFejvIMuoNWPIKo130_assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600335.RAOEYH4y96hZQcEpSjL3yKryrihXJZWFejvIMuoNWPIKo130_provenance.