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Matches in Nanopublications for { ?s ?p "[PRSS1 mutations were identified mainly in CP patients (9.6% of CP vs 2.5% of ARP alleles, P = 0.094), whereas N34S SPINK1 mutation was present with comparable frequency in CP and ARP patients (7.7% vs 10.0%, P = 0.768).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP273501.RAYlf7vspl46Dp3sboompUkT0jBSqU6FVDcfRMv6-pQ88130_assertion description "[PRSS1 mutations were identified mainly in CP patients (9.6% of CP vs 2.5% of ARP alleles, P = 0.094), whereas N34S SPINK1 mutation was present with comparable frequency in CP and ARP patients (7.7% vs 10.0%, P = 0.768).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP273501.RAYlf7vspl46Dp3sboompUkT0jBSqU6FVDcfRMv6-pQ88130_provenance.
• NP199944.RA_sPsko11PS-ozeId2UAOqSRS_PQB8o-3ViRPCCIaBr0130_assertion description "[PRSS1 mutations were identified mainly in CP patients (9.6% of CP vs 2.5% of ARP alleles, P = 0.094), whereas N34S SPINK1 mutation was present with comparable frequency in CP and ARP patients (7.7% vs 10.0%, P = 0.768).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199944.RA_sPsko11PS-ozeId2UAOqSRS_PQB8o-3ViRPCCIaBr0130_provenance.
• NP262891.RAI7qRbIFnIlCzvalIDWtxv53QPxHzdMSJhiMDrepH7SM130_assertion description "[PRSS1 mutations were identified mainly in CP patients (9.6% of CP vs 2.5% of ARP alleles, P = 0.094), whereas N34S SPINK1 mutation was present with comparable frequency in CP and ARP patients (7.7% vs 10.0%, P = 0.768).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262891.RAI7qRbIFnIlCzvalIDWtxv53QPxHzdMSJhiMDrepH7SM130_provenance.
• NP595215.RALNrOCoA1V4fJOJ7mzgP829Nroh6yDqjshrrbnnBrXTc130_assertion description "[PRSS1 mutations were identified mainly in CP patients (9.6% of CP vs 2.5% of ARP alleles, P = 0.094), whereas N34S SPINK1 mutation was present with comparable frequency in CP and ARP patients (7.7% vs 10.0%, P = 0.768).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP595215.RALNrOCoA1V4fJOJ7mzgP829Nroh6yDqjshrrbnnBrXTc130_provenance.
• assertion description "[PRSS1 mutations were identified mainly in CP patients (9.6% of CP vs 2.5% of ARP alleles, P = 0.094), whereas N34S SPINK1 mutation was present with comparable frequency in CP and ARP patients (7.7% vs 10.0%, P = 0.768).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[PRSS1 mutations were identified mainly in CP patients (9.6% of CP vs 2.5% of ARP alleles, P = 0.094), whereas N34S SPINK1 mutation was present with comparable frequency in CP and ARP patients (7.7% vs 10.0%, P = 0.768).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP710435.RAhaKtk2mRUbk2sWGN1gSGZcXRugV6OjkztWQYqMTG1z4130_assertion description "[PRSS1 mutations were identified mainly in CP patients (9.6% of CP vs 2.5% of ARP alleles, P = 0.094), whereas N34S SPINK1 mutation was present with comparable frequency in CP and ARP patients (7.7% vs 10.0%, P = 0.768).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710435.RAhaKtk2mRUbk2sWGN1gSGZcXRugV6OjkztWQYqMTG1z4130_provenance.
• NP567932.RArnzlVtf5z92avLYMdqI6GNnD4C2EAu7t6qeXK1tNDrY130_assertion description "[PRSS1 mutations were identified mainly in CP patients (9.6% of CP vs 2.5% of ARP alleles, P = 0.094), whereas N34S SPINK1 mutation was present with comparable frequency in CP and ARP patients (7.7% vs 10.0%, P = 0.768).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP567932.RArnzlVtf5z92avLYMdqI6GNnD4C2EAu7t6qeXK1tNDrY130_provenance.
• NP972188.RAGJd8XO2VsBVuL97u8dqdBo90S43ptSt3jBY-P8GUYBI130_assertion description "[PRSS1 mutations were identified mainly in CP patients (9.6% of CP vs 2.5% of ARP alleles, P = 0.094), whereas N34S SPINK1 mutation was present with comparable frequency in CP and ARP patients (7.7% vs 10.0%, P = 0.768).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP972188.RAGJd8XO2VsBVuL97u8dqdBo90S43ptSt3jBY-P8GUYBI130_provenance.
• NP649458.RA0hA84TlHocwV3NqBrImTbu8N6Z8l3R5thawuXssX8K4130_assertion description "[PRSS1 mutations were identified mainly in CP patients (9.6% of CP vs 2.5% of ARP alleles, P = 0.094), whereas N34S SPINK1 mutation was present with comparable frequency in CP and ARP patients (7.7% vs 10.0%, P = 0.768).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649458.RA0hA84TlHocwV3NqBrImTbu8N6Z8l3R5thawuXssX8K4130_provenance.
• NP567930.RAMoogKF2SUpZpkE_kdXl9fPa8-ZGuq4zFxYb277lvdtE130_assertion description "[PRSS1 mutations were identified mainly in CP patients (9.6% of CP vs 2.5% of ARP alleles, P = 0.094), whereas N34S SPINK1 mutation was present with comparable frequency in CP and ARP patients (7.7% vs 10.0%, P = 0.768).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP567930.RAMoogKF2SUpZpkE_kdXl9fPa8-ZGuq4zFxYb277lvdtE130_provenance.
• NP567933.RAP3F5hMhXT4oW2kJWs5rGVKju-2cgkGJnyEwd_BiejxA130_assertion description "[PRSS1 mutations were identified mainly in CP patients (9.6% of CP vs 2.5% of ARP alleles, P = 0.094), whereas N34S SPINK1 mutation was present with comparable frequency in CP and ARP patients (7.7% vs 10.0%, P = 0.768).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP567933.RAP3F5hMhXT4oW2kJWs5rGVKju-2cgkGJnyEwd_BiejxA130_provenance.
• NP567939.RAJGyRhn48SxYudMt1B5oUpUD4jzmeU94MXIPq19GUXuQ130_assertion description "[PRSS1 mutations were identified mainly in CP patients (9.6% of CP vs 2.5% of ARP alleles, P = 0.094), whereas N34S SPINK1 mutation was present with comparable frequency in CP and ARP patients (7.7% vs 10.0%, P = 0.768).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP567939.RAJGyRhn48SxYudMt1B5oUpUD4jzmeU94MXIPq19GUXuQ130_provenance.