Use my Search Websuite to scan PubMed, PMCentral, Journal Hosts and Journal Archives, FullText. Kick-your-searchterm to multiple Engines kick-your-query now !>

A dictionary by aggregated review articles of nephrology, medicine and the life sciences Your one-stop-run pathway from word to the immediate pdf of peer-reviewed on-topic knowledge.

10.1016/j.ajhg.2015.05.020 http://scihub22266oqcxt.onion/10.1016/j.ajhg.2015.05.020 C4572507!4572507!26119816     free     free     free Deprecated: Implicit conversion from float 235.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 235.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 235.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 235.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 235.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Am+J+Hum+Genet 2015 ; 97 (1): 111-24 Nephropedia Template TP {{tp|p=26119816|t=2015. The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease |pdf=|usr=}}{{26119816}} gab.com Text The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease JO: Am J Hum Genet http://www.kidney.de/pget.php?&tw=1&pmid=26119816 #FOAvip The Human Phenotype Ontology (HPO) is widely used in the rare disease community for differential diagnostics, phenotype-driven analysis of next-generation sequence-variation data, and translational research, but a comparable resource has not been available for common disease. Here, we have developed a concept-recognition procedure that analyzes the frequencies of HPO disease annotations as identified in over five million PubMed abstracts by employing an iterative procedure to optimize precision and recall of the identified terms. We derived disease models for 3,145 common human diseases comprising a total of 132,006 HPO annotations. The HPO now comprises over 250,000 phenotypic annotations for over 10,000 rare and common diseases and can be used for examining the phenotypic overlap among common diseases that share risk alleles, as well as between Mendelian diseases and common diseases linked by genomic location. The annotations, as well as the HPO itself, are freely available. Twit Text FOAVip The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease ????Am J Hum Genet http://www.kidney.de/pget.php?&tw=1&pmid=26119816 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26119816 #FOAvip English Wikipedia <ref>{{Cite pmid|26119816}}</ref> The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease #MMPMID26119816 Groza T; Köhler S; Moldenhauer D; Vasilevsky N; Baynam G; Zemojtel T; Schriml L; Kibbe W; Schofield P; Beck T; Vasant D; Brookes A; Zankl A; Washington N; Mungall C; Lewis S; Haendel MA; Parkinson H; Robinson P Am J Hum Genet 2015[Jul]; 97 (1): 111-24 PMID26119816show ga The Human Phenotype Ontology (HPO) is widely used in the rare disease community for differential diagnostics, phenotype-driven analysis of next-generation sequence-variation data, and translational research, but a comparable resource has not been available for common disease. Here, we have developed a concept-recognition procedure that analyzes the frequencies of HPO disease annotations as identified in over five million PubMed abstracts by employing an iterative procedure to optimize precision and recall of the identified terms. We derived disease models for 3,145 common human diseases comprising a total of 132,006 HPO annotations. The HPO now comprises over 250,000 phenotypic annotations for over 10,000 rare and common diseases and can be used for examining the phenotypic overlap among common diseases that share risk alleles, as well as between Mendelian diseases and common diseases linked by genomic location. The annotations, as well as the HPO itself, are freely available. äThe Human Phenotype Ontology: Semantic Unification of Common and Rare (epmc).pdf DeepDyve Pubget Overpricing