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83. Li MJ, Liu Z, Wang P, Wong MP, Nelson MR, Kocher JP et al (2016) GWASdb v2, an update
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84. Denny JC, Bastarache L, Ritchie MD, Carroll RJ, Zink R, Mosley JD et al (2013) Systematic
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85. Yu W, Gwinn M, Clyne M, Yesupriya A, Khoury MJ (2008) A navigator for human genome
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86. Pinero J, Queralt-Rosinach N, Bravo A, Deu-Pons J, Bauer-Mehren A, Baron M et al (2015)
DisGeNET, a discovery platform for the dynamical exploration of human diseases and their
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87. Bodenreider O (2004) The unified medical language system (UMLS), integrating biomedical
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95
69. Hornbeck PV, Zhang B, Murray B, Kornhauser JM, Latham V, Skrzypek E (2015) PhosphoSitePlus, 2014, mutations, PTMs and recalibrations. Nucleic Acids Res 43(Database
issue):D512–520
70. Lu CT, Huang KY, Su MG, Lee TY, Bretana NA, Chang WC et al (2013) DbPTM 3.0, an
informative resource for investigating substrate site specificity and functional association of
protein post-translational modifications. Nucleic Acids Res 41(Database issue):D295–305
71. Dinkel H, Chica C, Via A, Gould CM, Jensen LJ, Gibson TJ et al (2011) Phospho.ELM, a database of phosphorylation sites–update 2011. Nucleic Acids Res 39(Database
issue):D261–267
72. Fazekas D, Koltai M, Turei D, Modos D, Palfy M, Dul Z et al (2013) SignaLink 2—a signaling
pathway resource with multi-layered regulatory networks. BMC Syst Biol 7:7
73. Huttlin EL, Bruckner RJ, Paulo JA, Cannon JR, Ting L, Baltier K et al (2017) Architecture of the human interactome defines protein communities and disease networks. Nature
545(7655):505–509
74. Chatr-Aryamontri A, Breitkreutz BJ, Oughtred R, Boucher L, Heinicke S, Chen D et al
(2015) The BioGRID interaction database, 2015 update. Nucleic Acids Res 43(Database
issue):D470–478
75. Cowley MJ, Pinese M, Kassahn KS, Waddell N, Pearson JV, Grimmond SM et al (2012)
PINA v2.0, mining interactome modules. Nucleic Acids Res 40(Database issue):D862–865
76. Licata L, Briganti L, Peluso D, Perfetto L, Iannuccelli M, Galeota E et al (2012)
MINT, the molecular interaction database, 2012 update. Nucleic Acids Res 40(Database
issue):D857–861
77. Orchard S, Ammari M, Aranda B, Breuza L, Briganti L, Broackes-Carter F et al (2014)
The MIntAct project–IntAct as a common curation platform for 11 molecular interaction
databases. Nucleic Acids Res 42(Database issue):D358–363
78. Breuer K, Foroushani AK, Laird MR, Chen C, Sribnaia A, Lo R et al (2013) InnateDB,
systems biology of innate immunity and beyond–recent updates and continuing curation.
Nucleic Acids Res 41(Database issue):D1228–1233
79. Amberger JS, Bocchini CA, Schiettecatte F, Scott AF, Hamosh A (2015) OMIM.org, Online
Mendelian Inheritance in Man (OMIM(R)), an online catalog of human genes and genetic
disorders. Nucleic Acids Res 43(Database issue):D789–798
80. Davis AP, Grondin CJ, Lennon-Hopkins K, Saraceni-Richards C, Sciaky D, King BL et al
(2015) The comparative toxicogenomics database’s 10th year anniversary, update 2015.
Nucleic Acids Res 43(Database issue):D914–920
81. Landrum MJ, Lee JM, Riley GR, Jang W, Rubinstein WS, Church DM et al (2014) ClinVar,
public archive of relationships among sequence variation and human phenotype. Nucleic
Acids Res 42(Database issue):D980–985
82. Welter D, MacArthur J, Morales J, Burdett T, Hall P, Junkins H et al (2014) The NHGRI
GWAS Catalog, a curated resource of SNP-trait associations. Nucleic Acids Res 42(Database
issue):D1001–1006
83. Li MJ, Liu Z, Wang P, Wong MP, Nelson MR, Kocher JP et al (2016) GWASdb v2, an update
database for human genetic variants identified by genome-wide association studies. Nucleic
Acids Res 44(D1):D869–D876
84. Denny JC, Bastarache L, Ritchie MD, Carroll RJ, Zink R, Mosley JD et al (2013) Systematic
comparison of phenome-wide association study of electronic medical record data and genomewide association study data. Nat Biotechnol 31(12):1102–1110
85. Yu W, Gwinn M, Clyne M, Yesupriya A, Khoury MJ (2008) A navigator for human genome
epidemiology. Nat Genet 40(2):124–125
86. Pinero J, Queralt-Rosinach N, Bravo A, Deu-Pons J, Bauer-Mehren A, Baron M et al (2015)
DisGeNET, a discovery platform for the dynamical exploration of human diseases and their
genes. Database (Oxford), bav028
87. Bodenreider O (2004) The unified medical language system (UMLS), integrating biomedical
terminology. Nucleic Acids Res 32(Database issue):D267–270