Nanopublications LDF server

Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }

• NP93096.RAurCPwhDebjwfUbUpgAiNCFiTUhK1HG1zTtNf6NDL4y4130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93096.RAurCPwhDebjwfUbUpgAiNCFiTUhK1HG1zTtNf6NDL4y4130_provenance.
• NP93098.RAnIBWHEFqnRjpL-jw0ohltuN1lfev5v2y8ys8VkEAcVg130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93098.RAnIBWHEFqnRjpL-jw0ohltuN1lfev5v2y8ys8VkEAcVg130_provenance.
• NP93101.RAi0G2mGx8y2kY13Ecuiv95Z7hQNGg13ARu3g9RA9nlJg130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93101.RAi0G2mGx8y2kY13Ecuiv95Z7hQNGg13ARu3g9RA9nlJg130_provenance.
• NP93110.RAjBf55XaiPw60n1iCjV_S8z4b5TJ29VvyWVa7PCKmodE130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93110.RAjBf55XaiPw60n1iCjV_S8z4b5TJ29VvyWVa7PCKmodE130_provenance.
• NP93111.RAl5SiCve8YStNBF8Iis9nCnA8Tn2VoJoT-bf9wKL58Kc130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93111.RAl5SiCve8YStNBF8Iis9nCnA8Tn2VoJoT-bf9wKL58Kc130_provenance.
• NP93112.RAohzGWaz0giFgS_tZ1Nnzv3iFBZOmdfjxzzvb-UkTRCg130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93112.RAohzGWaz0giFgS_tZ1Nnzv3iFBZOmdfjxzzvb-UkTRCg130_provenance.
• NP93113.RAk_VlrZVOH4RiJBEr2CBWbaevTvrdIr7vnagNOVlGoaY130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93113.RAk_VlrZVOH4RiJBEr2CBWbaevTvrdIr7vnagNOVlGoaY130_provenance.
• NP93115.RAmekUkGKzP_2Oyyt5TlO11m0e52LPOwygdj2ESXsMVvU130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93115.RAmekUkGKzP_2Oyyt5TlO11m0e52LPOwygdj2ESXsMVvU130_provenance.
• NP93125.RAqSMmdf0ITjpcQhyQDHPvn9MrN5F6lGjbOqe7qehoxHY130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93125.RAqSMmdf0ITjpcQhyQDHPvn9MrN5F6lGjbOqe7qehoxHY130_provenance.
• NP93129.RAthPWxZDB-GHTp7DivjuUqPbaQa-zAubpMsVlD6U_7TI130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93129.RAthPWxZDB-GHTp7DivjuUqPbaQa-zAubpMsVlD6U_7TI130_provenance.
• NP93148.RArKDf8YWJAYTUnZuq7MUoH0jLcIvdaCBMP282TTh0HT0130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93148.RArKDf8YWJAYTUnZuq7MUoH0jLcIvdaCBMP282TTh0HT0130_provenance.
• NP93151.RAv8gl4AK0e8oisZzh524m4x9VFlCq_wuXfhwDNjz6XnE130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93151.RAv8gl4AK0e8oisZzh524m4x9VFlCq_wuXfhwDNjz6XnE130_provenance.
• NP93161.RAnFe6YU68pOioPjl--8-eGeAuKxpmfnpJa5SqGMH-NNM130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93161.RAnFe6YU68pOioPjl--8-eGeAuKxpmfnpJa5SqGMH-NNM130_provenance.
• NP93169.RAjUss062Ie6zRER1iTW4bjaw9VwDXcT5fVH8ubajAxPk130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93169.RAjUss062Ie6zRER1iTW4bjaw9VwDXcT5fVH8ubajAxPk130_provenance.
• NP93171.RAgLicm4uU_uQbq0NJNiejW7kxIuwNM9cAih06yR3SxMo130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93171.RAgLicm4uU_uQbq0NJNiejW7kxIuwNM9cAih06yR3SxMo130_provenance.
• NP93172.RAjfJ4DadtEi_P-hOTZ5iycn3MBqHXKs_bC4i5LTk0Feg130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93172.RAjfJ4DadtEi_P-hOTZ5iycn3MBqHXKs_bC4i5LTk0Feg130_provenance.
• NP93175.RAi9IypTAiwhRK6vKW7mBd3O-Ar3s4AZKrtFxV_ftLG9w130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93175.RAi9IypTAiwhRK6vKW7mBd3O-Ar3s4AZKrtFxV_ftLG9w130_provenance.
• NP93182.RAlyVkxia1qsYikP7e294-VkUeM1dc8jTrUUMirNvmmXU130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93182.RAlyVkxia1qsYikP7e294-VkUeM1dc8jTrUUMirNvmmXU130_provenance.
• NP93184.RArIePNqg0UsLIkLCuf9GcVnqylwY03VHV2ZMea6vFFU0130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93184.RArIePNqg0UsLIkLCuf9GcVnqylwY03VHV2ZMea6vFFU0130_provenance.
• NP93185.RAre1h2aWVLr9nsDWgyQnJvc2g4AGMy8tIodlj6B6RRog130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93185.RAre1h2aWVLr9nsDWgyQnJvc2g4AGMy8tIodlj6B6RRog130_provenance.
• NP93188.RAkE26by2ZRadbhhxD5AfQu8Wv3yzFUiFFHoyeEpFExKg130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93188.RAkE26by2ZRadbhhxD5AfQu8Wv3yzFUiFFHoyeEpFExKg130_provenance.
• NP93202.RAtq6xad8VsoGyGFrgl-HSA7wJRL2Lu6LDIS5Li7CUSqg130_assertion description "[A second-generation genomewide screen for asthma-susceptibility alleles in a founder population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93202.RAtq6xad8VsoGyGFrgl-HSA7wJRL2Lu6LDIS5Li7CUSqg130_provenance.
• NP93205.RAr1-WguEZBU-HMELfOGiTirKL_syvgBLKuTUEpMwdQL4130_assertion description "[A second-generation genomewide screen for asthma-susceptibility alleles in a founder population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93205.RAr1-WguEZBU-HMELfOGiTirKL_syvgBLKuTUEpMwdQL4130_provenance.
• NP93212.RAkjXHfZnY6MUGoh47GRt6usYQabT-OyXMwjRlwYtXu6E130_assertion description "[A second-generation genomewide screen for asthma-susceptibility alleles in a founder population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93212.RAkjXHfZnY6MUGoh47GRt6usYQabT-OyXMwjRlwYtXu6E130_provenance.
• NP93217.RAtv_TERwPAJNigqHq4wdMvu5mxM2xJCOdsnuvLe_bPhg130_assertion description "[A second-generation genomewide screen for asthma-susceptibility alleles in a founder population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93217.RAtv_TERwPAJNigqHq4wdMvu5mxM2xJCOdsnuvLe_bPhg130_provenance.
• NP93222.RAhqTwD3PoVDt7uxvq2q5ARCfcztwVcahbbricuxgpE_k130_assertion description "[A second-generation genomewide screen for asthma-susceptibility alleles in a founder population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93222.RAhqTwD3PoVDt7uxvq2q5ARCfcztwVcahbbricuxgpE_k130_provenance.
• NP93224.RAlWfeqjgmYD16UAE1CHeraEH3qEoC-2m04w-8xK6RnJk130_assertion description "[A second-generation genomewide screen for asthma-susceptibility alleles in a founder population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93224.RAlWfeqjgmYD16UAE1CHeraEH3qEoC-2m04w-8xK6RnJk130_provenance.
• NP93227.RAr_uQ09oF8Gsn9IOi-B2fVH0RkZsiAK05R1tGuS_51FQ130_assertion description "[A second-generation genomewide screen for asthma-susceptibility alleles in a founder population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93227.RAr_uQ09oF8Gsn9IOi-B2fVH0RkZsiAK05R1tGuS_51FQ130_provenance.
• NP93229.RArZ9g40KW7EwUUpgNndFknehgUFbqM-ICx2NvSSqxgQU130_assertion description "[A second-generation genomewide screen for asthma-susceptibility alleles in a founder population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93229.RArZ9g40KW7EwUUpgNndFknehgUFbqM-ICx2NvSSqxgQU130_provenance.
• NP93231.RApzfsfhrNUF7yVwSq3oFAEo-aDO2QTvaSMAnwbm2e9Lg130_assertion description "[A second-generation genomewide screen for asthma-susceptibility alleles in a founder population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93231.RApzfsfhrNUF7yVwSq3oFAEo-aDO2QTvaSMAnwbm2e9Lg130_provenance.
• NP93234.RAmVIbjFAb1ecRBl-rWGCf-IgkwraFl_dzifaEi5Utrq0130_assertion description "[A second-generation genomewide screen for asthma-susceptibility alleles in a founder population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93234.RAmVIbjFAb1ecRBl-rWGCf-IgkwraFl_dzifaEi5Utrq0130_provenance.
• NP93236.RAvHkT5bij5-oAtFb2mlJx280smAcj6K8gsad9LK8LFYA130_assertion description "[A second-generation genomewide screen for asthma-susceptibility alleles in a founder population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93236.RAvHkT5bij5-oAtFb2mlJx280smAcj6K8gsad9LK8LFYA130_provenance.
• NP93239.RAq6u9i3RudlphaTOjmPnYwd8XjjL1MRxPnW68p6eAnI4130_assertion description "[These findings suggested that multiple genetic polymorphisms of CTNNA3 may be determinants of susceptibility to TDI-induced asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93239.RAq6u9i3RudlphaTOjmPnYwd8XjjL1MRxPnW68p6eAnI4130_provenance.
• NP93241.RAulFgaXJ_33aiGomTCFaUdpg-E_q7LbOS_v6l9uZQn2A130_assertion description "[A second-generation genomewide screen for asthma-susceptibility alleles in a founder population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93241.RAulFgaXJ_33aiGomTCFaUdpg-E_q7LbOS_v6l9uZQn2A130_provenance.
• NP93243.RAo9ATCHgCrt1TzU86LHX1QNpbS3FJj0fZPXlt0uclzNI130_assertion description "[A second-generation genomewide screen for asthma-susceptibility alleles in a founder population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93243.RAo9ATCHgCrt1TzU86LHX1QNpbS3FJj0fZPXlt0uclzNI130_provenance.
• NP93248.RAsWWuwh78qh8IybscaLbLQvohM8VJ5e1qH9ZSCQWNq7E130_assertion description "[A second-generation genomewide screen for asthma-susceptibility alleles in a founder population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93248.RAsWWuwh78qh8IybscaLbLQvohM8VJ5e1qH9ZSCQWNq7E130_provenance.
• NP93251.RAmHjdVn47HMGalcOxIgEAtylObSQjKoRYw_jsgXbjLbE130_assertion description "[High-resolution whole-genome association study of Parkinson disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93251.RAmHjdVn47HMGalcOxIgEAtylObSQjKoRYw_jsgXbjLbE130_provenance.
• NP93255.RAvlT6T2nOSGweEkbumNR3eysuGNHhCBJW6mEPGfb3pyA130_assertion description "[High-resolution whole-genome association study of Parkinson disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93255.RAvlT6T2nOSGweEkbumNR3eysuGNHhCBJW6mEPGfb3pyA130_provenance.
• NP93259.RAkg02hXmIuWP_rock_r1G2_Gy0Op3Wr4ltPzKmmCzDZg130_assertion description "[High-resolution whole-genome association study of Parkinson disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93259.RAkg02hXmIuWP_rock_r1G2_Gy0Op3Wr4ltPzKmmCzDZg130_provenance.
• NP93260.RApECPaB4KqZCO0-GPGcVBrcYixBR4gRvRJqKQ-85pc8I130_assertion description "[High-resolution whole-genome association study of Parkinson disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93260.RApECPaB4KqZCO0-GPGcVBrcYixBR4gRvRJqKQ-85pc8I130_provenance.
• NP93269.RAhyzL6TNjNeVtNWHr5oizAL35vX9wu8EVJm8XhBefTWU130_assertion description "[High-resolution whole-genome association study of Parkinson disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93269.RAhyzL6TNjNeVtNWHr5oizAL35vX9wu8EVJm8XhBefTWU130_provenance.
• NP93270.RAnKUbyLruky8EYaK4YvDsJ2FwyFkoehY0APWG5-I9mr4130_assertion description "[High-resolution whole-genome association study of Parkinson disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93270.RAnKUbyLruky8EYaK4YvDsJ2FwyFkoehY0APWG5-I9mr4130_provenance.
• NP93279.RAqVdTJt2A1DroO82p305ustb_dXIXxPmW1LAPFs0T5Nc130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93279.RAqVdTJt2A1DroO82p305ustb_dXIXxPmW1LAPFs0T5Nc130_provenance.
• NP93287.RAhBo8FSklN6Ow9Vz52Hu7xIIbW9ooPMBr2UYABnJYxbs130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93287.RAhBo8FSklN6Ow9Vz52Hu7xIIbW9ooPMBr2UYABnJYxbs130_provenance.
• NP93288.RAtaAnzbFr6QiNYGV-jnJZs1fuWg8jEaSzuHd0poDHrz0130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93288.RAtaAnzbFr6QiNYGV-jnJZs1fuWg8jEaSzuHd0poDHrz0130_provenance.
• NP93291.RArQG14Uv1nzv6mSA-14Mm4067b4Jv8d0wD2RFVZ-g_4Y130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93291.RArQG14Uv1nzv6mSA-14Mm4067b4Jv8d0wD2RFVZ-g_4Y130_provenance.
• NP93292.RAuFJe1OYkCS4LaU-MkUjJQYvYZG42_k0f9_VuUOWtHKY130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93292.RAuFJe1OYkCS4LaU-MkUjJQYvYZG42_k0f9_VuUOWtHKY130_provenance.
• NP93295.RAqayuOOw4Eai-zMLpPUT_gV_euSvsDpe8C2BVvDGooTg130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93295.RAqayuOOw4Eai-zMLpPUT_gV_euSvsDpe8C2BVvDGooTg130_provenance.
• NP93298.RAl0b4uTTwc1mXLDIOwOBA_ftex_jKiSf0HvgUKSatIL4130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93298.RAl0b4uTTwc1mXLDIOwOBA_ftex_jKiSf0HvgUKSatIL4130_provenance.
• NP93300.RAi8ni-BEta1zcbU9jJIgB6Jz-ky-EAHktLXeTfbRnzsA130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93300.RAi8ni-BEta1zcbU9jJIgB6Jz-ky-EAHktLXeTfbRnzsA130_provenance.
• NP93302.RAkqhMSP9I_Ub3pFmJ1nXmmrCMpx1VYC4TX1NJNJhr9os130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93302.RAkqhMSP9I_Ub3pFmJ1nXmmrCMpx1VYC4TX1NJNJhr9os130_provenance.
• NP93305.RAqapJdRzVgcGlphfH6IEj_BCgvU7C3Oe0U8MD2ssywYI130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93305.RAqapJdRzVgcGlphfH6IEj_BCgvU7C3Oe0U8MD2ssywYI130_provenance.
• NP93308.RArqz_IlGIb2Z6ZkvHmxnlZafLU9B6BqmDrvsqhrVX0_I130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93308.RArqz_IlGIb2Z6ZkvHmxnlZafLU9B6BqmDrvsqhrVX0_I130_provenance.
• NP93312.RAgr-fuxO_vgRI-oOxGaAltyplMj6Z4Gm1hPit4QRAs3w130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93312.RAgr-fuxO_vgRI-oOxGaAltyplMj6Z4Gm1hPit4QRAs3w130_provenance.
• NP93314.RAk4bak8cKT6lbAKqrUf2X9qYOOJK5SMbnoqYmli8zR28130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93314.RAk4bak8cKT6lbAKqrUf2X9qYOOJK5SMbnoqYmli8zR28130_provenance.
• NP93325.RAqapTbg4mAwp-i4UWZ9xdf7rxDt2krfZgVE8nqqL-WZ8130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93325.RAqapTbg4mAwp-i4UWZ9xdf7rxDt2krfZgVE8nqqL-WZ8130_provenance.
• NP93327.RAupC4ZVsasgrjA2tePE9drAG9ceid4xiikSocQe2iMPg130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93327.RAupC4ZVsasgrjA2tePE9drAG9ceid4xiikSocQe2iMPg130_provenance.
• NP93337.RAg4DpPydN61OwuRY4-le8iSC7uLlDGoT0Iv0Vl1GCL0o130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93337.RAg4DpPydN61OwuRY4-le8iSC7uLlDGoT0Iv0Vl1GCL0o130_provenance.
• NP93345.RAp_lPDwgtaFil5YtBjI2NJIDOJCPCZSK2BDxv5H20n7Y130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93345.RAp_lPDwgtaFil5YtBjI2NJIDOJCPCZSK2BDxv5H20n7Y130_provenance.
• NP93349.RAgM2ASNG1KlWykVCdQv-1A5OvPuwgiS6KVpx2fxibP9g130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93349.RAgM2ASNG1KlWykVCdQv-1A5OvPuwgiS6KVpx2fxibP9g130_provenance.
• NP93350.RAllQQx_nfxZmYpboM18BWke3foXeyKZG2xaXHKe8dHDs130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93350.RAllQQx_nfxZmYpboM18BWke3foXeyKZG2xaXHKe8dHDs130_provenance.
• NP93352.RApC2UmX0O5MbhySMF46cEzLebp-p93Q1YLnGHdJ8iTWA130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93352.RApC2UmX0O5MbhySMF46cEzLebp-p93Q1YLnGHdJ8iTWA130_provenance.
• NP93356.RAoQB2bDt_iuc3OOKf6NGkDXOeiZAYzybJ6y5Tp5M-BCM130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93356.RAoQB2bDt_iuc3OOKf6NGkDXOeiZAYzybJ6y5Tp5M-BCM130_provenance.
• NP93363.RAsHkylWISjiec8xH4yJFDrPfefynmYTCqcLVW8iwXJzg130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93363.RAsHkylWISjiec8xH4yJFDrPfefynmYTCqcLVW8iwXJzg130_provenance.
• NP93364.RAqcdJ7mZRXAw4Ejrf2tE0_Pnga7x_Fhc2g5oGcwQoTtI130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93364.RAqcdJ7mZRXAw4Ejrf2tE0_Pnga7x_Fhc2g5oGcwQoTtI130_provenance.
• NP93366.RAmlDqDDsq9pCQ10OzF6fq2Vk1IVPyRhbz0amYvt26CxY130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93366.RAmlDqDDsq9pCQ10OzF6fq2Vk1IVPyRhbz0amYvt26CxY130_provenance.
• NP93369.RAneNRujQd8btT3POu1RkugaYYJ9pypQtvqatx-fRHTEU130_assertion description "[We generated publicly available genotype data for Parkinsons disease patients and controls so that these data can be mined and augmented by other researchers to identify common genetic variability that results in minor and moderate risk for disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93369.RAneNRujQd8btT3POu1RkugaYYJ9pypQtvqatx-fRHTEU130_provenance.
• NP93380.RAua4sQVvoS06Ob6Pg0Xz_i5yvRCLfIM6A8Kq3Z4e82FE130_assertion description "[A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93380.RAua4sQVvoS06Ob6Pg0Xz_i5yvRCLfIM6A8Kq3Z4e82FE130_provenance.
• NP93383.RAgh2xrKg7BNGsjTGL5NcnIEgoJm4Mg0jixlytZ4D-tcU130_assertion description "[A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93383.RAgh2xrKg7BNGsjTGL5NcnIEgoJm4Mg0jixlytZ4D-tcU130_provenance.
• NP93384.RAqPsvUX319aPGenkx6wVOma9yxskSw3Ij24vTbtWvNxU130_assertion description "[A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93384.RAqPsvUX319aPGenkx6wVOma9yxskSw3Ij24vTbtWvNxU130_provenance.
• NP93389.RAucZRDCAJJlEyl46KHWbAfpuILYhnmsVMsRESJcLv7KM130_assertion description "[A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93389.RAucZRDCAJJlEyl46KHWbAfpuILYhnmsVMsRESJcLv7KM130_provenance.
• NP93395.RAn-brQsYEVOI_etlM85bvOdNF2P8-np4jWCtFwuhhCWA130_assertion description "[A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93395.RAn-brQsYEVOI_etlM85bvOdNF2P8-np4jWCtFwuhhCWA130_provenance.
• NP93403.RAqhFnUbp9qNpQMKraIPrPKcmzSI95s_2lFVCyH6h3-S0130_assertion description "[A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93403.RAqhFnUbp9qNpQMKraIPrPKcmzSI95s_2lFVCyH6h3-S0130_provenance.
• NP93405.RAkYI9sYsJ0ApqBicY-R4_EckGr48uXqqO21e2Xaie9AU130_assertion description "[A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93405.RAkYI9sYsJ0ApqBicY-R4_EckGr48uXqqO21e2Xaie9AU130_provenance.
• NP93408.RAqT5eyfe3YfV7Y8dJR44Q76fMKSbeqR0pMDfh26XI5Wc130_assertion description "[A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93408.RAqT5eyfe3YfV7Y8dJR44Q76fMKSbeqR0pMDfh26XI5Wc130_provenance.
• NP93409.RAuZ5u2Xkp-hzdbrX91DjqAMoIHTHiM-IZDdq4i-uAt-w130_assertion description "[A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93409.RAuZ5u2Xkp-hzdbrX91DjqAMoIHTHiM-IZDdq4i-uAt-w130_provenance.
• NP93410.RAqIamQBd98PKDB1asy9EnsKsYTbRR6MBR04B3IE9pwhQ130_assertion description "[A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93410.RAqIamQBd98PKDB1asy9EnsKsYTbRR6MBR04B3IE9pwhQ130_provenance.
• NP93411.RAgvSSMo48ognqr82bmMZiydi2GlK8bgAMfbRjrJQNK9Q130_assertion description "[A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93411.RAgvSSMo48ognqr82bmMZiydi2GlK8bgAMfbRjrJQNK9Q130_provenance.
• NP93413.RAkJVJMAXzoBrg5TvdsuWylYw97S1pciU8ED4BxufQhfY130_assertion description "[A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93413.RAkJVJMAXzoBrg5TvdsuWylYw97S1pciU8ED4BxufQhfY130_provenance.
• NP93415.RAr0Gp48xnx_WsANgpYiNtSWUdMXITQ3vZz7NXVldbOOw130_assertion description "[Common variants at five new loci associated with early-onset inflammatory bowel disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93415.RAr0Gp48xnx_WsANgpYiNtSWUdMXITQ3vZz7NXVldbOOw130_provenance.
• NP93417.RAiIk1B5Ic8LIlp-6PBazhnVKOskdMOqVN4xNPnrDeUfo130_assertion description "[A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93417.RAiIk1B5Ic8LIlp-6PBazhnVKOskdMOqVN4xNPnrDeUfo130_provenance.
• NP93419.RAq3Lwab7qNLRfGuvvj2rk2z1eVaz3GFGPa7t9WS42uIk130_assertion description "[A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93419.RAq3Lwab7qNLRfGuvvj2rk2z1eVaz3GFGPa7t9WS42uIk130_provenance.
• NP93420.RAlnaf6vQDr_p2a70wBlSVddlmS2ONvxLW02JnAydElF4130_assertion description "[A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93420.RAlnaf6vQDr_p2a70wBlSVddlmS2ONvxLW02JnAydElF4130_provenance.
• NP93424.RAkWlPZWrsIDuu-sVUpgqPx-WtWFj2ztgHX-nfReni5kw130_assertion description "[A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93424.RAkWlPZWrsIDuu-sVUpgqPx-WtWFj2ztgHX-nfReni5kw130_provenance.
• NP93425.RAjtUno8C0-Q3N9W7Atn7aFffoPKTPf05DtqP_cA-40zg130_assertion description "[A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93425.RAjtUno8C0-Q3N9W7Atn7aFffoPKTPf05DtqP_cA-40zg130_provenance.
• NP93427.RAp_hbXRpDqrZxbg68br8fCsDW1UzCgJG_DpT8kC8BK10130_assertion description "[A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93427.RAp_hbXRpDqrZxbg68br8fCsDW1UzCgJG_DpT8kC8BK10130_provenance.
• NP93429.RAmXZmQc-IREiudAEOzQP9HDcB3eEgCkOX8hBYsJUSHuM130_assertion description "[A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93429.RAmXZmQc-IREiudAEOzQP9HDcB3eEgCkOX8hBYsJUSHuM130_provenance.
• NP93431.RAizjFPqnKLvRmJQywC5ryKLg7gGukdML6HNjGq-dNc54130_assertion description "[A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93431.RAizjFPqnKLvRmJQywC5ryKLg7gGukdML6HNjGq-dNc54130_provenance.
• NP93432.RAqGvJ--zUgUE5h5Zgfjw6ym-qmWzLdl6iIofh76yG8so130_assertion description "[A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93432.RAqGvJ--zUgUE5h5Zgfjw6ym-qmWzLdl6iIofh76yG8so130_provenance.
• NP93433.RAhen2cMsSyv-ZnY8_Pfz6OoGn39Uyq5NtvhcnriCqJbI130_assertion description "[A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93433.RAhen2cMsSyv-ZnY8_Pfz6OoGn39Uyq5NtvhcnriCqJbI130_provenance.
• NP93445.RAkC5tqSOu3VpoAlQQKNB3TZbo5JZGuYef9zEQOi2zn9E130_assertion description "[We generated publicly available genotype data for sporadic ALS patients and controls. No single locus was definitively associated with increased risk of developing disease, although potentially associated candidate SNPs were identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93445.RAkC5tqSOu3VpoAlQQKNB3TZbo5JZGuYef9zEQOi2zn9E130_provenance.
• NP93448.RAohAKlCV6jFmOnEL3I78fpf90g2AGs1GbRP-SKGCQDbg130_assertion description "[We generated publicly available genotype data for sporadic ALS patients and controls. No single locus was definitively associated with increased risk of developing disease, although potentially associated candidate SNPs were identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93448.RAohAKlCV6jFmOnEL3I78fpf90g2AGs1GbRP-SKGCQDbg130_provenance.
• NP93452.RArX1gAKWlY94tSeatCyVDISILFd88d3JN-ugYZv-zPBM130_assertion description "[We generated publicly available genotype data for sporadic ALS patients and controls. No single locus was definitively associated with increased risk of developing disease, although potentially associated candidate SNPs were identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93452.RArX1gAKWlY94tSeatCyVDISILFd88d3JN-ugYZv-zPBM130_provenance.
• NP93454.RAsJzB29KW2LWCrQG1xxRIoxQCX94KO26KM0XHW9s6tPM130_assertion description "[We generated publicly available genotype data for sporadic ALS patients and controls. No single locus was definitively associated with increased risk of developing disease, although potentially associated candidate SNPs were identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93454.RAsJzB29KW2LWCrQG1xxRIoxQCX94KO26KM0XHW9s6tPM130_provenance.
• NP93458.RAtheALO-oeZl0AK05_iHhW1XUSp6FDCug-LkywiN1gs0130_assertion description "[We generated publicly available genotype data for sporadic ALS patients and controls. No single locus was definitively associated with increased risk of developing disease, although potentially associated candidate SNPs were identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93458.RAtheALO-oeZl0AK05_iHhW1XUSp6FDCug-LkywiN1gs0130_provenance.
• NP93464.RAjzR6rW94gf-HVBem0OgIeCKZ01Et2ZhkUoMpLIKE3ws130_assertion description "[We generated publicly available genotype data for sporadic ALS patients and controls. No single locus was definitively associated with increased risk of developing disease, although potentially associated candidate SNPs were identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93464.RAjzR6rW94gf-HVBem0OgIeCKZ01Et2ZhkUoMpLIKE3ws130_provenance.
• NP93470.RAs4lYA2Iz9EQwDp54Mm-jzR7gZ_EK1T0ub4NhNg7JV5g130_assertion description "[We generated publicly available genotype data for sporadic ALS patients and controls. No single locus was definitively associated with increased risk of developing disease, although potentially associated candidate SNPs were identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93470.RAs4lYA2Iz9EQwDp54Mm-jzR7gZ_EK1T0ub4NhNg7JV5g130_provenance.
• NP93473.RAg3E5gEOkKd-yA1qgF6G6KJRngt8ctbyVJPY2CrOKMWQ130_assertion description "[We generated publicly available genotype data for sporadic ALS patients and controls. No single locus was definitively associated with increased risk of developing disease, although potentially associated candidate SNPs were identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93473.RAg3E5gEOkKd-yA1qgF6G6KJRngt8ctbyVJPY2CrOKMWQ130_provenance.
• NP93476.RAqQyDdk_x06b00muQS-NyrDkrzzot3bWAb-4TpyMrwGc130_assertion description "[We generated publicly available genotype data for sporadic ALS patients and controls. No single locus was definitively associated with increased risk of developing disease, although potentially associated candidate SNPs were identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93476.RAqQyDdk_x06b00muQS-NyrDkrzzot3bWAb-4TpyMrwGc130_provenance.
• NP93477.RAjgN2sKtEub3sivcVlG11x9vIb7fn8uwq3Yehe2Sm2sU130_assertion description "[We generated publicly available genotype data for sporadic ALS patients and controls. No single locus was definitively associated with increased risk of developing disease, although potentially associated candidate SNPs were identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93477.RAjgN2sKtEub3sivcVlG11x9vIb7fn8uwq3Yehe2Sm2sU130_provenance.

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