PhenomicDB: a new cross-species genotype/phenotype resource
about
Linking human diseases to animal models using ontology-based phenotype annotationMining phenotypes for gene function predictionPhenoclustering: online mining of cross-species phenotypesMouse genetic and phenotypic resources for human geneticsThe landscape of microbial phenotypic traits and associated genesResources for functional genomics studies in Drosophila melanogasterToward knowledge support for analysis and interpretation of complex traitsPhenoHM: human-mouse comparative phenome-genome server.A bioinformatics expert system linking functional data to anatomical outcomes in limb regenerationCMGSDB: integrating heterogeneous Caenorhabditis elegans data sources using compositional data mining.Integrating mouse anatomy and pathology ontologies into a phenotyping database: tools for data capture and trainingIntegrating phenotype and gene expression data for predicting gene function.Using association rule mining to determine promising secondary phenotyping hypothesesPhenotype ontologies for mouse and man: bridging the semantic gap.MouseFinder: Candidate disease genes from mouse phenotype data.PhenomeNET: a whole-phenome approach to disease gene discovery.Selection of extreme phenotypes: the role of clinical observation in translational research.Planform: an application and database of graph-encoded planarian regenerative experiments.Inference of gene-phenotype associations via protein-protein interaction and orthology.Organ system heterogeneity DB: a database for the visualization of phenotypes at the organ system levelNew approaches to the representation and analysis of phenotype knowledge in human diseases and their animal modelsInter-functional analysis of high-throughput phenotype data by non-parametric clustering and its application to photosynthesis.Accelerating Adverse Outcome Pathway Development Using Publicly Available Data Sources.Towards a bioinformatics of patterning: a computational approach to understanding regulative morphogenesisNeurocarta: aggregating and sharing disease-gene relations for the neurosciences.Array comparative genomic hybridization and computational genome annotation in constitutional cytogenetics: suggesting candidate genes for novel submicroscopic chromosomal imbalance syndromes.The evolution of human genetic studies of cleft lip and cleft palate.The digital revolution in phenotyping.Computational tools for comparative phenomics: the role and promise of ontologies.ProtozoaDB 2.0: A Trypanosoma Brucei Case Study.Modular organization of the human disease genes: a text-based network inferenceTowards a Pathway Inventory of the Human Brain for Modeling Disease Mechanisms Underlying Neurodegeneration.Experimental models for anxiolytic drug discovery in the era of omes and omics.Bar charts detection and analysis in biomedical literature of PubMed Central.
P2860
Q21145806-C2322D2E-627F-4069-9D31-D134FAB5238DQ21284209-33E0B6DA-C59C-4C57-A812-19C81FEF6E17Q24607538-0AE91CF2-6C2B-4208-87B4-9B30F2567297Q24628817-0CFC6A4D-4486-4EC1-833C-B2471A6FAC8FQ28589802-8ED8AD5E-1F6C-4CDB-89CC-BA186DC557AAQ28657863-AFD529AF-4575-45C7-9073-7E111067AC9CQ28658388-0D2B28F5-BC37-471F-AD32-836D3245897FQ30484528-545A5B85-9E55-49D0-B6F8-6000A36B2092Q30902179-98B9A4E9-200B-411C-A28E-BD15A481F12BQ31133365-59289042-04AA-41C2-9D9F-4BDD84EF3F37Q33370116-ABE15374-17F1-4123-BBB5-9DA4F6A0A50EQ33509214-74409674-5D78-426C-817E-6B7C801DEF74Q33760921-308DFEC5-AD6B-4647-8898-03A1728D6545Q33815395-046EACBB-403C-4581-BF16-C9CAEA804580Q34158189-EA26AEFA-F3EF-458E-A0AA-78FCC176E547Q34198496-57FCAF0A-2079-4CBB-BFC8-19DF67F83848Q34384968-A8501401-BF8E-4583-AB5D-FDB6A495B944Q34593616-5F384335-A686-4C3E-96F5-EB11BCB72D6CQ35032445-ACBE7E4F-0E16-47B3-AF15-B7E6621F312BQ35254821-841AE202-028F-49DF-94F7-678316BA1816Q35296454-A4C618FF-CBE1-4175-B0F1-2908CACF9EDAQ35765215-68C142ED-08ED-4D20-9E6F-B93B1A9EF69FQ35904173-9099E66D-7C11-41C1-9AD9-6166383E09B0Q36619289-A91FDE9F-6F17-4156-90C0-3C9F49BBA983Q36691322-5CE4CF0B-11F3-448F-82A0-1056116AACA5Q36943655-8529DEF3-C855-4C9C-9BC2-B62676B727C4Q37139817-4903F3B2-9295-48C2-986F-E1B475CDF316Q37284033-FD511404-3A09-4C07-A19F-6EDD264CB228Q38027771-5342F276-60AB-46BC-BC88-06BD32BFB06AQ38670651-9D3B4F7E-0BEB-44FF-B6CF-0C16EA7DD50CQ38946957-96752581-D32F-469E-861D-3891712C6287Q39850175-E204B95C-E4F2-4B7B-8780-EA0F81F3D4FFQ45854291-13B593A5-8A85-4868-9F81-F689701D8841Q55395612-2D99CB9A-9AA2-48E7-9DD4-381DF5EB7162
P2860
PhenomicDB: a new cross-species genotype/phenotype resource
description
2007 nî lūn-bûn
@nan
2007 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
PhenomicDB: a new cross-species genotype/phenotype resource
@ast
PhenomicDB: a new cross-species genotype/phenotype resource
@en
PhenomicDB: a new cross-species genotype/phenotype resource
@nl
type
label
PhenomicDB: a new cross-species genotype/phenotype resource
@ast
PhenomicDB: a new cross-species genotype/phenotype resource
@en
PhenomicDB: a new cross-species genotype/phenotype resource
@nl
prefLabel
PhenomicDB: a new cross-species genotype/phenotype resource
@ast
PhenomicDB: a new cross-species genotype/phenotype resource
@en
PhenomicDB: a new cross-species genotype/phenotype resource
@nl
P2093
P2860
P356
P1476
PhenomicDB: a new cross-species genotype/phenotype resource
@en
P2093
Bertram Weiss
Georgi Georgiev
Hans-Dieter Pohlenz
Ivan Kalev
Nadia Pavlova
Philip Groth
Spas Tonov
P2860
P304
P356
10.1093/NAR/GKL662
P407
P433
Database issue
P577
2007-01-01T00:00:00Z