Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP65404.RAmur2uOyjnX4hmN1pwulERWqth1Um0XJKxvwST-LtSLw130_assertion description "[We found evidence that diabetes and obesity risk alleles interact with maternal pregravid body mass index to predict gestational weight gain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65404.RAmur2uOyjnX4hmN1pwulERWqth1Um0XJKxvwST-LtSLw130_provenance.
- NP65405.RAq-JX50mq2jYDJwC8vt7d-JuUa_QZe7bZnMYxgCQoUL8130_assertion description "[The results demonstrated that genetic variation in KCNJ11, BDNF, PFKP, PTER and SEC16B were associated with SGA and support the concept that genetic factors associated with obesity and/or type 2 diabetes are more prevalent in those born SGA compared to those born AGA. We have previously determined that environmental factors are associated with differences in birthweight in the ABC study and now we have demonstrated a significant genetic contribution, suggesting that the interaction between genetics and the environment are important.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65405.RAq-JX50mq2jYDJwC8vt7d-JuUa_QZe7bZnMYxgCQoUL8130_provenance.
- NP65409.RAmhkfZxGCt2WN8Ks-OZhR-uMXgCN0C9ZwG1GotgZ4Qqc130_assertion description "[We hypothesized that functional polymorphisms in the insulin pathway genes INS, INSR, IGFBPI, insulin receptor substrate 1 (IRS1), and IRS2 may be associated with CRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65409.RAmhkfZxGCt2WN8Ks-OZhR-uMXgCN0C9ZwG1GotgZ4Qqc130_provenance.
- NP65411.RAq1Q_uJSk-LEKN7KP65SPQS27g-HfbuqLdT32CPQRU6A130_assertion description "[Toll-like receptor signaling pathway variants and prostate cancer mortality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65411.RAq1Q_uJSk-LEKN7KP65SPQS27g-HfbuqLdT32CPQRU6A130_provenance.
- NP65412.RAlTfuRRSYNi4C22eSSZKXBsIYGSE3sc1n1P5JSmS3Pj0130_assertion description "[Our data suggest a mechanistic link between hyperactivation of the innate immune system and chronic airway inflammation and indicate IRAK-M as a potential target for therapeutic intervention against asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65412.RAlTfuRRSYNi4C22eSSZKXBsIYGSE3sc1n1P5JSmS3Pj0130_provenance.
- NP65413.RAh3QC6oct22mumlwQ58WfdJ17DuRmJsSy2I6G_EoDPXs130_assertion description "[To investigate whether polymorphisms in these genes were associated with asthma or asthma-related phenotypes, we screened these genes for polymorphisms by direct sequencing of 24 asthmatics and identified 19 variants in IRAK-M and 12 variants in SIGIRR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65413.RAh3QC6oct22mumlwQ58WfdJ17DuRmJsSy2I6G_EoDPXs130_provenance.
- NP65414.RAvEHhlUi8xtpx9ZsK17EQiJvPAydfLjm6nZgUToLj2Uk130_assertion description "[Interactions of sequence variants in interleukin-1 receptor-associated kinase4 and the toll-like receptor 6-1-10 gene cluster increase prostate cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65414.RAvEHhlUi8xtpx9ZsK17EQiJvPAydfLjm6nZgUToLj2Uk130_provenance.
- NP65415.RAt4T68ECfnUQ4zpxEUHx0CAG4HMetDx7UqI0uyyBOUm8130_assertion description "[Toll-like receptor signaling pathway variants and prostate cancer mortality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65415.RAt4T68ECfnUQ4zpxEUHx0CAG4HMetDx7UqI0uyyBOUm8130_provenance.
- NP65423.RAvCJJl3wGf2BDfZN12FE0SqP71xrCHvQmXsDK61y6lMU130_assertion description "[We evaluated the effect of polymorphisms in four insulin-related genes (G972R in IRS1, G1057D in IRS2, a CA repeat in IGFI and an A/C polymorphism at -202 of IGFBP3) on the risk of microsatellite instability and KRAS2 and TP53 mutations in a population-based set of 1788 cases of colon cancer and 1981 controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65423.RAvCJJl3wGf2BDfZN12FE0SqP71xrCHvQmXsDK61y6lMU130_provenance.
- NP65441.RAp1F5ecNnKC4VRiStJBqFXoJZ0rMQ_MeajjzuVFdaT-Q130_assertion description "[Association and gene-gene interaction of SLC6A4 and ITGB3 in autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65441.RAp1F5ecNnKC4VRiStJBqFXoJZ0rMQ_MeajjzuVFdaT-Q130_provenance.
- NP65444.RAmWxY8RkQivoIwJuLpbhIwzNHgoiN9Ro3Di2lUuc51DE130_assertion description "[A functional SNP in ITIH3 is associated with susceptibility to myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65444.RAmWxY8RkQivoIwJuLpbhIwzNHgoiN9Ro3Di2lUuc51DE130_provenance.
- NP65446.RAhOvfJqEtDY9cWliUHBQr6Kw6SPz6nGqtXCY7oLC4w4c130_assertion description "[Polymorphisms in the AMPD1, ATIC, and ITPA genes are associated with good clinical response to MTX treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65446.RAhOvfJqEtDY9cWliUHBQr6Kw6SPz6nGqtXCY7oLC4w4c130_provenance.
- NP65451.RAgtFNEH30AZqDLdBXcXuBmYMAbhKCQ0Yeh5DEewVbVi4130_assertion description "[The incidence of the JAK2 V617F mutation in patients with idiopathic erythrocytosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65451.RAgtFNEH30AZqDLdBXcXuBmYMAbhKCQ0Yeh5DEewVbVi4130_provenance.
- NP65456.RAr3yQawkWYypyU6d1GGUv-xxjz4HqP33di3sSpwfWu98130_assertion description "[Detection of JAK2V617F mutation and its clinical significance in 80 patients with M2 acute myelogenous leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65456.RAr3yQawkWYypyU6d1GGUv-xxjz4HqP33di3sSpwfWu98130_provenance.
- NP65457.RApZzvcv23xMhE3vCifwSv7XqXU4OJzMx7FFPKtre-9u8130_assertion description "[Positive association of schizophrenia to JARID2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65457.RApZzvcv23xMhE3vCifwSv7XqXU4OJzMx7FFPKtre-9u8130_provenance.
- NP65462.RAttdEaDWzrtgnHWjYNbzxmAroFjKasn2RFo04WxvSIg8130_assertion description "[In this large cohort of unrelated patients referred for LQTS genetic testing, the clinical phenotype strongly correlated with the likelihood of elucidating a pathogenic mutation with the cardiac channel gene screen.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65462.RAttdEaDWzrtgnHWjYNbzxmAroFjKasn2RFo04WxvSIg8130_provenance.
- NP65465.RAi53ar1AFm2kwNnvVmLDmzICI3Bgn812Tcvcv0p9Ltb8130_assertion description "[KCNH2 K897T and rs3807375 as well as the four studied NOS1AP variants have modest effects on ECG TPE interval but are not related to T-wave morphology measures. The previously observed prognostic value of T-wave morphology parameters likely is not based on these SNPs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65465.RAi53ar1AFm2kwNnvVmLDmzICI3Bgn812Tcvcv0p9Ltb8130_provenance.
- NP65471.RAml1AMDwNE41k0_1zVj_jxCwZhBvMXwG1YwncDKweeOY130_assertion description "[Retrospective analysis of the first 2,500 cases (1,515 female patients, average age at testing 23 +/- 17 years, range 0 to 90 years) scanned for mutations in 5 of the LQTS-susceptibility genes: KCNQ1 (LQT1), KCNH2 (LQT2), SCN5A (LQT3), KCNE1 (LQT5), and KCNE2 (LQT6).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65471.RAml1AMDwNE41k0_1zVj_jxCwZhBvMXwG1YwncDKweeOY130_provenance.
- NP65477.RAr1u92bdI5txpMuZhlFoY0fw9wikQN5JFi2uHfnxGOWY130_assertion description "[Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65477.RAr1u92bdI5txpMuZhlFoY0fw9wikQN5JFi2uHfnxGOWY130_provenance.
- NP65478.RAq8XwY27p2P1sBGtoJepIlch8mXOM6rCmpZiyQzQihcA130_assertion description "[In total, 592 unrelated German IGE patients and 462 healthy population controls were genotyped for the delA750 truncation mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65478.RAq8XwY27p2P1sBGtoJepIlch8mXOM6rCmpZiyQzQihcA130_provenance.
- NP65479.RAuRta2kQB4jNyXt8JgujB3ILlxbq6dW834YNWrYH318k130_assertion description "[The single nucleotide polymorphisms of I(Ks) potassium channel genes and their association with atrial fibrillation in a Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65479.RAuRta2kQB4jNyXt8JgujB3ILlxbq6dW834YNWrYH318k130_provenance.
- NP65481.RAlUi3PbJAI5MjKUJKMwQitqMi3ljBW_TcyfF__P9YdIo130_assertion description "[The present study demonstrated that genetic variations of VEGFR2 are significantly associated with atopy in the Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65481.RAlUi3PbJAI5MjKUJKMwQitqMi3ljBW_TcyfF__P9YdIo130_provenance.
- NP65482.RAmXULmPlsRuL5MZz2P5AN2THux-Poa9wKH1tkCOYPcaY130_assertion description "[Polymorphisms in the KDR and POSTN genes: association with breast cancer susceptibility and prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65482.RAmXULmPlsRuL5MZz2P5AN2THux-Poa9wKH1tkCOYPcaY130_provenance.
- NP65487.RAssIRWYtP6VqdjMWcgxwzRAGvNrfCUNfMJqUrGnm7H1g130_assertion description "[HLA-C and KIR genes in hepatitis C virus infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65487.RAssIRWYtP6VqdjMWcgxwzRAGvNrfCUNfMJqUrGnm7H1g130_provenance.
- NP65489.RAgMwjtTAYLTBNTDaDM5RgJzc9svi_Hc4pRzAHC1D6wd4130_assertion description "[this study suggests that the activating KIR2DS4 may serve as CML susceptive gene to trigger leukemia development, while KIR2DS3 is possibly a protect gene of ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65489.RAgMwjtTAYLTBNTDaDM5RgJzc9svi_Hc4pRzAHC1D6wd4130_provenance.
- NP65493.RApauoQ5sEoarVocZHLIvoabZ8S6a2xumHzfwWWP41JUc130_assertion description "[Interaction of KIR genes and G1M immunoglobulin allotypes confer susceptibility to type 2 diabetes in Puerto Rican Americans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65493.RApauoQ5sEoarVocZHLIvoabZ8S6a2xumHzfwWWP41JUc130_provenance.
- NP65494.RAg112bAyBqD4CMWWYe8OBWha5lvVC-msrsLcvbw8bUck130_assertion description "[Genetic interactions of KIR and G1M immunoglobulin allotypes differ in obese from non-obese individuals with type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65494.RAg112bAyBqD4CMWWYe8OBWha5lvVC-msrsLcvbw8bUck130_provenance.
- NP65495.RAoMokoAWTq2T6Bsl-zUJhZA6TUkEem_15mrz9YlFHgXQ130_assertion description "[Polymorphism of killer cell immunoglobulin-like receptor gene and its correlation with leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65495.RAoMokoAWTq2T6Bsl-zUJhZA6TUkEem_15mrz9YlFHgXQ130_provenance.
- NP65499.RAg21Xo3FxjMDTte0xvRX8gKCTGXKcOOP2ePpv7jNyKuU130_assertion description "[Polymorphism of killer cell immunoglobulin-like receptor gene and its correlation with leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65499.RAg21Xo3FxjMDTte0xvRX8gKCTGXKcOOP2ePpv7jNyKuU130_provenance.
- NP65500.RAkYan9g8JJdwkjreAjwb-A2xIDfdbSbvLVDy_JVS13OI130_assertion description "[this study suggests that the activating KIR2DS4 may serve as CML susceptive gene to trigger leukemia development, while KIR2DS3 is possibly a protect gene of ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65500.RAkYan9g8JJdwkjreAjwb-A2xIDfdbSbvLVDy_JVS13OI130_provenance.
- NP65501.RAnk8_leaYmiGPCtybrmDxyfSIHxlKnbrutdKXWDVHuvE130_assertion description "[Killer Ig-like receptor (KIR) genotype and HLA ligand combinations in ulcerative colitis susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65501.RAnk8_leaYmiGPCtybrmDxyfSIHxlKnbrutdKXWDVHuvE130_provenance.
- NP65502.RAjr_JBLs_YfzlUqJX_OrWBYBswikAnMnl_kQYDrXCBMk130_assertion description "[Polymorphism of killer cell immunoglobulin-like receptor gene and its correlation with leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65502.RAjr_JBLs_YfzlUqJX_OrWBYBswikAnMnl_kQYDrXCBMk130_provenance.
- NP65507.RAuG-HkNx4QzUvM3VJ83oqcuc812j1-VACxASnwA5qj8w130_assertion description "[Interaction of KIR genes and G1M immunoglobulin allotypes confer susceptibility to type 2 diabetes in Puerto Rican Americans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65507.RAuG-HkNx4QzUvM3VJ83oqcuc812j1-VACxASnwA5qj8w130_provenance.
- NP65511.RAjB2EZHlSgP4E8oMA7uLYndNii0G66US-Cz5e-Iabj7E130_assertion description "[the effect of the KIR genes on psoriasis susceptibility is complex, extending beyond the association with KIR2DS1 and involving protective effects and interactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65511.RAjB2EZHlSgP4E8oMA7uLYndNii0G66US-Cz5e-Iabj7E130_provenance.
- NP65514.RAm38Vgg5SfiPZyxU5UP0PMO5LP-9pCNRAPIXjq9llckw130_assertion description "[Polymorphism of killer cell immunoglobulin-like receptor gene and its correlation with leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65514.RAm38Vgg5SfiPZyxU5UP0PMO5LP-9pCNRAPIXjq9llckw130_provenance.
- NP65515.RAu63pdNcQI1WDClQyJCc3H-RXKeqvEQ5vWwt82U6pjj0130_assertion description "[this study suggests that the activating KIR2DS4 may serve as CML susceptive gene to trigger leukemia development, while KIR2DS3 is possibly a protect gene of ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65515.RAu63pdNcQI1WDClQyJCc3H-RXKeqvEQ5vWwt82U6pjj0130_provenance.
- NP65521.RAihreFEl12oJ9sMYkQKADZLWcUVpcx-bIadQ6c22cy_c130_assertion description "[this study suggests that the activating KIR2DS4 may serve as CML susceptive gene to trigger leukemia development, while KIR2DS3 is possibly a protect gene of ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65521.RAihreFEl12oJ9sMYkQKADZLWcUVpcx-bIadQ6c22cy_c130_provenance.
- NP65522.RAmt0xTwBYG7bh61XQ7rM9cSTIf8DdHBq8wxHgo9aReAk130_assertion description "[Polymorphism of killer cell immunoglobulin-like receptor gene and its correlation with leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65522.RAmt0xTwBYG7bh61XQ7rM9cSTIf8DdHBq8wxHgo9aReAk130_provenance.
- NP65528.RAkNvbAlt_sUZe8XbTRTpxmrQc5rQRX3yR6Xdk2dpaTYM130_assertion description "[Our data indicate that the KIT/KITLG system may be involved in a low sperm count trait in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65528.RAkNvbAlt_sUZe8XbTRTpxmrQc5rQRX3yR6Xdk2dpaTYM130_provenance.
- NP65529.RApA1ysX2smMaHUsGb-LH-JE5Z09WlSljRvhNfv79YOEY130_assertion description "[We investigated the association of polymorphisms in klotho with ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65529.RApA1ysX2smMaHUsGb-LH-JE5Z09WlSljRvhNfv79YOEY130_provenance.
- NP65534.RAsxbgfIMIY2OXBo5hIxqAX48TDN80-2VPSH_JfHJRofM130_assertion description "[Identification of the NKG2D haplotypes associated with natural cytotoxic activity of peripheral blood lymphocytes and cancer immunosurveillance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65534.RAsxbgfIMIY2OXBo5hIxqAX48TDN80-2VPSH_JfHJRofM130_provenance.
- NP65535.RAgpmzBVh8oZ7_KJWiq__qf8i56crj3z8Br4E1Uwh00r8130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65535.RAgpmzBVh8oZ7_KJWiq__qf8i56crj3z8Br4E1Uwh00r8130_provenance.
- NP65536.RAk8vTDA_MkMDe9O5I9ohy3HPyHQK2v_TTC3bKKn5YEo4130_assertion description "[Association study between kynurenine 3-monooxygenase gene and schizophrenia in the Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65536.RAk8vTDA_MkMDe9O5I9ohy3HPyHQK2v_TTC3bKKn5YEo4130_provenance.
- NP65546.RAp3Bdg_ccpq-K6heasiVHM_y3yjj_UJyOfkhbo9-Xj48130_assertion description "[Association of common LH variant with hyperfunctional promoter in a Japanese infertile woman.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65546.RAp3Bdg_ccpq-K6heasiVHM_y3yjj_UJyOfkhbo9-Xj48130_provenance.
- NP65550.RAtMvbWRUy5ogzsnDM9afliiLr8oRiPvDK4KE5RKa5PDw130_assertion description "[DNA repair and cell cycle control genes and the risk of young-onset lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65550.RAtMvbWRUy5ogzsnDM9afliiLr8oRiPvDK4KE5RKa5PDw130_provenance.
- NP65553.RAmttI2h4i2gN536ZLh1-85UjgwgsEekVIEBLhQ9Z4GIk130_assertion description "[In order to examine the association of common genetic variation in the base-excision repair (BER) pathway with bladder cancer risk, we analyzed 43 single nucleotide polymorphisms (SNPs) in 12 BER genes (OGG1, MUTYH, APEX1, PARP1, PARP3, PARP4, XRCC1, POLB, POLD1, PCNA, LIG1, and LIG3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65553.RAmttI2h4i2gN536ZLh1-85UjgwgsEekVIEBLhQ9Z4GIk130_provenance.
- NP65557.RArSeDYAIbKmmoMeZEFbIhQD7Gul8w17ofwJMAN5Hg6Hk130_assertion description "[In order to examine the association of common genetic variation in the base-excision repair (BER) pathway with bladder cancer risk, we analyzed 43 single nucleotide polymorphisms (SNPs) in 12 BER genes (OGG1, MUTYH, APEX1, PARP1, PARP3, PARP4, XRCC1, POLB, POLD1, PCNA, LIG1, and LIG3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65557.RArSeDYAIbKmmoMeZEFbIhQD7Gul8w17ofwJMAN5Hg6Hk130_provenance.
- NP65559.RAnXxjDIFYe72iHz4NIhJikeSg9b1TXwCnbsf0lzivL90130_assertion description "[In this study, we identified SNPs in LIG4, ERCC2, and CYP2D6 genes as putative markers to predict individuals at risk for complications arising from radiation therapy in prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65559.RAnXxjDIFYe72iHz4NIhJikeSg9b1TXwCnbsf0lzivL90130_provenance.
- NP65560.RAl1fJVHnaFHfAYUqo2BnX_vmtMahhSfZkEiaF3Sr8I3M130_assertion description "[Risk of non-Hodgkin lymphoma (NHL) in relation to germline variation in DNA repair and related genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65560.RAl1fJVHnaFHfAYUqo2BnX_vmtMahhSfZkEiaF3Sr8I3M130_provenance.
- NP65565.RAtIT8nmAf1GpuRrwv-YmYA9JYpXple5j8TfuuiLPj2UY130_assertion description "[one SNP of LOXL2 showed a significant association with IA individually, and we also detected a gene-gene interaction of LOXL2 with ELN/LIMK1, which may play an important role in susceptibility to IA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65565.RAtIT8nmAf1GpuRrwv-YmYA9JYpXple5j8TfuuiLPj2UY130_provenance.
- NP65566.RAuTKxKCes0w5F8N5sonoXblzB65g8IS8QATrcrin66JU130_assertion description "[The W81R was not found in our sample, but the M75T mutation was present in 43% of patients with coronary artery disease and 23% of age-matched controls. The genotype TT conferred a significant risk for myocardial infarction (odds ratio 2.53). This association was not due to linkage disequilibrium with kringle IV repeats. The M75T polymorphism was not associated with the LBS function of apo(a), but it influenced plasma Lp(a) concentration. ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65566.RAuTKxKCes0w5F8N5sonoXblzB65g8IS8QATrcrin66JU130_provenance.
- NP65567.RAhWMWYGqhap_-YpNPcZBGhIK9A30W32gsT-FATrAdDio130_assertion description "[Although APO (a) PNR, APO CI and APO CII genes are analyzed in only few populations, they show a frequency distribution, which is not at variance with that of APO E gene and other widely studied genetic markers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65567.RAhWMWYGqhap_-YpNPcZBGhIK9A30W32gsT-FATrAdDio130_provenance.
- NP65570.RArHUnebXYKUOoloX6rSaL-fnDHDMRc3OXcee_luorOEA130_assertion description "[Although a comparable healthy Israeli population study is needed for more precise interpretation of these results, frequency differences in these polymorphic alleles--associated with lipid metabolism, renin-angiotensin system and leukocyte adhesion mechanism--between CVD patients and healthy individuals nevertheless implicate these candidate genes as predisposing for CVD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65570.RArHUnebXYKUOoloX6rSaL-fnDHDMRc3OXcee_luorOEA130_provenance.
- NP65572.RAnQDoIXhgBVwZ5CF12nb59D4k-PqdjFNdT8j6gkHkHIA130_assertion description "[in this cohort of Chinese Canadians, the serum lipid profiles were more favorable than what has been reported for Caucasian Canadians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65572.RAnQDoIXhgBVwZ5CF12nb59D4k-PqdjFNdT8j6gkHkHIA130_provenance.
- NP65580.RAumi3_ZdKZ01gdxGlNzhZg0l7vMiVnDI4LFosyjeuPw4130_assertion description "[Low-density lipoprotein receptor-related protein 5 variant Q89R is associated with hypertension in Japanese females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65580.RAumi3_ZdKZ01gdxGlNzhZg0l7vMiVnDI4LFosyjeuPw4130_provenance.
- NP65581.RAvzNn5Ya62cLgJiwskXJtwLcu9kU1c6ZfqinqqA0Y2W8130_assertion description "[Common genetic variation within the low-density lipoprotein receptor-related protein 6 and late-onset Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65581.RAvzNn5Ya62cLgJiwskXJtwLcu9kU1c6ZfqinqqA0Y2W8130_provenance.
- NP65584.RAm-cH_6BaTkexGk9QdyEi-bwqm0GL9mF42MCy1ZckB7E130_assertion description "[The LRPAP1 insertion/deletion polymorphism is not associated with gallstone disease in a Polish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65584.RAm-cH_6BaTkexGk9QdyEi-bwqm0GL9mF42MCy1ZckB7E130_provenance.
- NP65585.RAmD_FV0Cbw277g8U-7FM8Yp8Mg0e5yVNznpthnU5oSgY130_assertion description "[Association of low density lipoprotein receptor related protein-associated protein (LRPAP1) gene insertion/deletion polymorphism with gallstone disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65585.RAmD_FV0Cbw277g8U-7FM8Yp8Mg0e5yVNznpthnU5oSgY130_provenance.
- NP65586.RAkfJH327dSlaKdO4oDXlYfCmEBn0v_RbR_hhaOmrrGM0130_assertion description "[LRPAP1, II genotype carrier females may have increased risk for gallstone disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65586.RAkfJH327dSlaKdO4oDXlYfCmEBn0v_RbR_hhaOmrrGM0130_provenance.
- NP65594.RAvzGqbYS3hIzAwVCWYUCs3TY2tX1IB21XU8hESmtyhLs130_assertion description "[Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65594.RAvzGqbYS3hIzAwVCWYUCs3TY2tX1IB21XU8hESmtyhLs130_provenance.
- NP65601.RAvHsxItMk3oh5RwkGy3inlMXHKJAsG6hb96_vNvAlmAY130_assertion description "[Although our findings require confirmation, we found suggestive evidence that genetic susceptibility modifies the positive association of birth weight with breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65601.RAvHsxItMk3oh5RwkGy3inlMXHKJAsG6hb96_vNvAlmAY130_provenance.
- NP65602.RApRvC28mfZ3Ife2opQUa-huYYu4PaNIFuwscZ8MfDYdk130_assertion description "[Association of breast cancer susceptibility variants with risk of pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65602.RApRvC28mfZ3Ife2opQUa-huYYu4PaNIFuwscZ8MfDYdk130_provenance.
- NP65606.RAohqdm0IH9CgXqxSx7kLkdsgq9wexLnI-hbjxlI2Xme8130_assertion description "[TNF-beta(+252) genotypes were significantly associated with MS: The frequency of TNF-beta 2,2 was increased (p = 0.00009) while the frequency of TNF-beta 1,2 was decreased (p = 0.0012) in MS patients as compared to controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65606.RAohqdm0IH9CgXqxSx7kLkdsgq9wexLnI-hbjxlI2Xme8130_provenance.
- NP65607.RAl1Hbx7dzhPoDQuPtSbFxsgNq93xmIS71NGZfzRzzzSc130_assertion description "[TNF-alpha, TNF-beta and IL-4 gene polymorphisms in Iranian patients with multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65607.RAl1Hbx7dzhPoDQuPtSbFxsgNq93xmIS71NGZfzRzzzSc130_provenance.
- NP65609.RAuqaV3_58LFx-2o8KJTnFu48TML--ZwV-906r2zGPoCQ130_assertion description "[TNF gene polymorphism has no effect on EMS in Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65609.RAuqaV3_58LFx-2o8KJTnFu48TML--ZwV-906r2zGPoCQ130_provenance.
- NP65612.RAvHKs7cpnGaEkZyfziQcE-lgx04TyxCPEsvnfdT8qG9U130_assertion description "[our findings suggest that polymorphisms in TGFB1 and LTA/TNF, and possibly other immune function genes, may influence susceptibility to TGCT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65612.RAvHKs7cpnGaEkZyfziQcE-lgx04TyxCPEsvnfdT8qG9U130_provenance.
- NP65614.RAiO4tpihvHWrhDwsDILBFKAzeNNEUwg205k4SIs1SMzg130_assertion description "[Polymorphisms of TNF-alpha and LT-alpha genes in multiple myeloma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65614.RAiO4tpihvHWrhDwsDILBFKAzeNNEUwg205k4SIs1SMzg130_provenance.
- NP65618.RAmnMwBzMcIFvvfm4PNYqQi-kC5rxDoQ5airjN-2ikhvM130_assertion description "[The C allele of the leukotriene C4 synthase gene increases the risk of developing allergic rhinitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65618.RAmnMwBzMcIFvvfm4PNYqQi-kC5rxDoQ5airjN-2ikhvM130_provenance.
- NP65630.RAh7qVjPwe_-Dc00dfU0c5grych-NjdDLSeNYCqF80j5U130_assertion description "[These genetic differences could be explained by various genes, the HTR1B, encoding the 5-HT(1) receptor subtype, MAOA gene that encodes the monoamino-oxidase, the main metabolic enzyme of this triptan, SLC6A4 (gene encoding the serotonin transporter) and DRD(2) (gene encoding the D(2) receptor), both involved in the pathogenesis of migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65630.RAh7qVjPwe_-Dc00dfU0c5grych-NjdDLSeNYCqF80j5U130_provenance.
- NP65631.RAre_7wQXw4-NfHtRYSymiz0nnqbOSh_gb2wps58_Qeuw130_assertion description "[Association study of the serotoninergic system in migraine in the Spanish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65631.RAre_7wQXw4-NfHtRYSymiz0nnqbOSh_gb2wps58_Qeuw130_provenance.
- NP65633.RAt1Iv-v28SfHiJ-vI95hK9WMHwPJnzwPtN05XmBFlaNQ130_assertion description "[Polymorphisms in genes regulating the HPA axis associated with empirically delineated classes of unexplained chronic fatigue.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65633.RAt1Iv-v28SfHiJ-vI95hK9WMHwPJnzwPtN05XmBFlaNQ130_provenance.
- NP65643.RApAC8UXYfmZ2wlfU-jC1aSHn6CnBqO06Y1MCX_6nyZKw130_assertion description "[Common genetic variants associated with breast cancer and mammographic density measures that predict disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65643.RApAC8UXYfmZ2wlfU-jC1aSHn6CnBqO06Y1MCX_6nyZKw130_provenance.
- NP65645.RAs5Mhb17hoHsfblgYASIxhlobglvYBtwPIdLwgZhPJN0130_assertion description "[Evaluation of 11 breast cancer susceptibility loci in African-American women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65645.RAs5Mhb17hoHsfblgYASIxhlobglvYBtwPIdLwgZhPJN0130_provenance.
- NP65651.RArVXcPcclemQtZ-Kb8fNmyyn-nFLNUWh9nccQttXpFZY130_assertion description "[The MBD4 Glu346Lys genotypes were determined in 432 lung cancer patients and 432 healthy age- and gender-matched control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65651.RArVXcPcclemQtZ-Kb8fNmyyn-nFLNUWh9nccQttXpFZY130_provenance.
- NP65652.RArZ7GXsMCDvpT4kDB-x0MpzD0XIpKYeBuEvBRXYWxIbs130_assertion description "[Tagging single nucleotide polymorphisms in MBD4 are associated with risk of lung cancer in a Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65652.RArZ7GXsMCDvpT4kDB-x0MpzD0XIpKYeBuEvBRXYWxIbs130_provenance.
- NP65654.RAnDulc3WHVSJwSIyHkgSpn-wGJz17IgKGguxLN93ebeA130_assertion description "[Comprehensive analysis of DNA repair gene polymorphisms and survival in patients with early stage non-small-cell lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65654.RAnDulc3WHVSJwSIyHkgSpn-wGJz17IgKGguxLN93ebeA130_provenance.
- NP65655.RAu0OkEgnADrXG5TdrKjJvPMiGBmVLiVbWWT2AmC9RuZM130_assertion description "[MBL deficiency is associated with ASCA positivity not only in patients with CD, but also in their relatives.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65655.RAu0OkEgnADrXG5TdrKjJvPMiGBmVLiVbWWT2AmC9RuZM130_provenance.
- NP65658.RAlQOxNYPM0JivZGY7gvNNkOPNUYt_OCnwwLVQym8_jcI130_assertion description "[MC1R and PTCH gene polymorphism in French patients with basal cell carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65658.RAlQOxNYPM0JivZGY7gvNNkOPNUYt_OCnwwLVQym8_jcI130_provenance.
- NP65664.RAtxONryJKnXjZY7QmTvzC_bOKx5Z3V9Edskf7owQGLmE130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65664.RAtxONryJKnXjZY7QmTvzC_bOKx5Z3V9Edskf7owQGLmE130_provenance.
- NP65673.RAiJ8upcOxBUoy8TzwmLpYlEaDoxhzEBpBzwCtRqTyjKQ130_assertion description "[A meta-analysis of the association of the HOPA12bp polymorphism and schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65673.RAiJ8upcOxBUoy8TzwmLpYlEaDoxhzEBpBzwCtRqTyjKQ130_provenance.
- NP65677.RAuc9aj5WfVGkovBzy9EGKyL62Eys5PxjcHDhyY4lURw0130_assertion description "[Recently, several genome-wide and candidate gene association studies have identified many novel genetic loci for type 2 diabetes (T2D); among these genes, CDKAL1, IGF2BP2, SLC30A8, CDKN2A/B, HHEX, FTO, TCF2, KCNQ1, and WFS1 are the most important.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65677.RAuc9aj5WfVGkovBzy9EGKyL62Eys5PxjcHDhyY4lURw0130_provenance.
- NP65683.RAsqhUAAx4ckruSgrOHb4JNy0zq-Wk5Dd2oj7azCNgiOg130_assertion description "[Individuals carrying T2D risk alleles of CDKAL1 or SLC30A8 had lower fasting plasma insulin level (rs7756992 P = 0.003) or lower basal insulin secretion (rs13266634 P = 0.0005), respectively, than non-carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65683.RAsqhUAAx4ckruSgrOHb4JNy0zq-Wk5Dd2oj7azCNgiOg130_provenance.
- NP65684.RAk6-H0u7hslIUeK7OEoUxH2DDac4IofDn2RvIj0gjtuQ130_assertion description "[Eight SNPs in five loci were found to be associated with type 2 diabetes: rs3802177 odds ratio (OR) = 1.16 (95% confidence interval (CI) 1.05-1.27); P = 4.5 x 10(-3) in SLC30A8; rs1111875 OR = 1.27 (95% CI 1.14-1.40); P = 1.4 x 10(-5) and rs7923837 OR = 1.27 (95% CI 1.13-1.43); P = 1.0 x 10(-4) in HHEX; rs10811661 OR = 1.27 (95% CI 1.15-1.40); P = 1.9 x 10(-6) in CDKN2B; rs4402960 OR = 1.23 (95% CI 1.11-1.36); P = 8.1 x 10(-5) and rs1470579 OR = 1.18 (95% CI 1.07-1.31); P = 8.3 x 10(-4) in IGF2BP2; and rs7754840 OR = 1.28 (95% CI 1.17-1.41); P = 4.5 x 10(-7) and rs7756992 OR = 1.27 (95% CI 1.15-1.40); P = 9.8 x 10(-7) in CDKAL1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65684.RAk6-H0u7hslIUeK7OEoUxH2DDac4IofDn2RvIj0gjtuQ130_provenance.
- NP65691.RAp1yT_2lwTwxy4CP4zg9_jHNwiDK76eRiIfz0GnYW3a4130_assertion description "[Although the overall effect of DNA repair genes in colorectal cancer etiology seems limited, their influence in the response to chemotherapy and prognosis may be more relevant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65691.RAp1yT_2lwTwxy4CP4zg9_jHNwiDK76eRiIfz0GnYW3a4130_provenance.
- NP65692.RAlG73r_QPVJoCEGuP3G0VFr95ARIbiLKu2IZmY-RO_zI130_assertion description "[Our results suggest that the common Leu84Phe and Ile143Val polymorphisms in MGMT influence risk of colorectal cancer in women possibly through modulating estrogen receptor-dependent transcriptional activation, which has previously been shown to occur in response to DNA alkylation damage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65692.RAlG73r_QPVJoCEGuP3G0VFr95ARIbiLKu2IZmY-RO_zI130_provenance.
- NP65696.RAlT_A0XrH3Phr3xNxjNUc_vE08F8o9zVKgFyFbQZU8cw130_assertion description "[DNA repair single-nucleotide polymorphisms in colorectal cancer and their role as modifiers of the effect of cigarette smoking and alcohol in the Singapore Chinese Health Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65696.RAlT_A0XrH3Phr3xNxjNUc_vE08F8o9zVKgFyFbQZU8cw130_provenance.
- NP65699.RAi4hU-PtHmiHvOsZnsgLxxCYokBwP-YALjXfdtUFiuI0130_assertion description "[However, the XRCC1(194) polymorphism had a significant interaction with the APE1(148) (p=0.005) or MGMT(84) polymorphism (p=0.02) in modifying the risk of pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65699.RAi4hU-PtHmiHvOsZnsgLxxCYokBwP-YALjXfdtUFiuI0130_provenance.
- NP65702.RAnTWW4ZK2FAdYU7T9zv6o0Al69szBzWb3DxbYEuw3-gg130_assertion description "[We demonstrate that this mutation co-segregated with the disease phenotype within a Chinese family affected with psoriasis vulgaris and is predicted to have an impact on the normal function of MGST2 protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65702.RAnTWW4ZK2FAdYU7T9zv6o0Al69szBzWb3DxbYEuw3-gg130_provenance.
- NP65711.RAotv6Bu20OO_Mpu3MfNT50RqNsyPyDqM1PG8C0GUgFqY130_assertion description "[Polymorphisms in MICB are associated with human herpes virus seropositivity and schizophrenia risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65711.RAotv6Bu20OO_Mpu3MfNT50RqNsyPyDqM1PG8C0GUgFqY130_provenance.
- NP65712.RAickxT-S407q-B-dg0fVgpaChKbfEAY3CV2325OinVdc130_assertion description "[The aim of this study was to evaluate the potential association of functional polymorphisms of macrophage migration inhibitory factor with systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65712.RAickxT-S407q-B-dg0fVgpaChKbfEAY3CV2325OinVdc130_provenance.
- NP65725.RArSV9x1660kyEz4UR5YXNcBH8ShrvPFiFrv2zlknSARo130_assertion description "[The level of association found in this study is in agreement with the nature of a complex genetic disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65725.RArSV9x1660kyEz4UR5YXNcBH8ShrvPFiFrv2zlknSARo130_provenance.
- NP65732.RAuG_G3L3bwh4uCU4HThTGgSnWNiLUpg0WeHedw8V1z-g130_assertion description "[For MMP-2, MMP-3, MMP-9, MMP-12, and TIMP-1 polymorphisms there were no clear associations with aneurysm growth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65732.RAuG_G3L3bwh4uCU4HThTGgSnWNiLUpg0WeHedw8V1z-g130_provenance.
- NP65737.RApPpt0YphC7tieF1dXrS9D-YMIviQbKDU-cCD6rDbOiA130_assertion description "[Using a case-only study, we examined the association of 11 single-nucleotide polymorphisms and one microsatellite polymorphism in MMP genes MMP1, MMP2, MMP3, MMP8, MMP9, and MMP12 with the risk of invasive bladder cancer in 243 Caucasian patients with muscle invasive compared with 315 Caucasian patients with superficial disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65737.RApPpt0YphC7tieF1dXrS9D-YMIviQbKDU-cCD6rDbOiA130_provenance.
- NP65738.RApZHAe45Zxc1-WTmi3Ky_3VH63XI4gnI_7wRKIb7m9bY130_assertion description "[It is suggested that the TIMP2 -418G to C gene polymorphism is associated with G-AgP in the Chinese subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65738.RApZHAe45Zxc1-WTmi3Ky_3VH63XI4gnI_7wRKIb7m9bY130_provenance.
- NP65740.RApj5yJUXS78s9P_D9VjKIUHN5s_uHtkz1fCYUAlF1aYc130_assertion description "[Matrix metalloproteinase-2, -9, and -12 gene polymorphisms in generalized aggressive periodontitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65740.RApj5yJUXS78s9P_D9VjKIUHN5s_uHtkz1fCYUAlF1aYc130_provenance.
- NP65744.RAm5a-JVgLNqu3wcz2tx0FC_0k6YJFBpUcgGf_u0qx_Ew130_assertion description "[Matrix metalloproteinase-9 gene -1562C/T polymorphism mitigates preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65744.RAm5a-JVgLNqu3wcz2tx0FC_0k6YJFBpUcgGf_u0qx_Ew130_provenance.
- NP65749.RAobyARUI-BVkzOrfX-FJDe3OEEQyuqgaII5h1UhsaEwQ130_assertion description "[Since angiotensin-converting enzyme (ACE) and matrix metalloproteinase (MMP) share the same homology, we investigated whether the MMP-3 and ACE I/D gene variants are involved in migraine risk and whether the ACE variant might act in combination with the MMP-3 genetic variant in patients with migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65749.RAobyARUI-BVkzOrfX-FJDe3OEEQyuqgaII5h1UhsaEwQ130_provenance.
- NP65751.RAsx7U0yT0UL9v0seuXTKmblvXQGUTcoTeVUr453twUTg130_assertion description "[Aberrant MMP-9 expression is closely related to tumor invasiveness and the prognosis of head and neck cancers. However, functional MMP-9-1562 C>T polymorphism is associated with OSCC risk only in younger areca chewers. The impact of aging or areca-related effect on this functional polymorphism should be elucidated. J Oral Pathol Med (2007).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65751.RAsx7U0yT0UL9v0seuXTKmblvXQGUTcoTeVUr453twUTg130_provenance.
- NP65752.RAn_CvbjZ0Y7oSBty9PPrxu3yZj8LIlw_nn-lHtn0kyEc130_assertion description "[Genetic variations in the MMP-7 and -9 gene may be part of a complex genetic risk profile to develop gastric ulcer in chronic H. pylori infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65752.RAn_CvbjZ0Y7oSBty9PPrxu3yZj8LIlw_nn-lHtn0kyEc130_provenance.
- NP65762.RAp086vFbvFvDkEkBxCxT8b1wh-H4-TMhZ_VSoFwTaHbs130_assertion description "[It is suggested that the TIMP2 -418G to C gene polymorphism is associated with G-AgP in the Chinese subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65762.RAp086vFbvFvDkEkBxCxT8b1wh-H4-TMhZ_VSoFwTaHbs130_provenance.