Browse using
OpenLink Faceted Browser
OpenLink Structured Data Editor
LodLive Browser
Formats
RDF:
N-Triples
N3
Turtle
JSON
XML
OData:
Atom
JSON
Microdata:
JSON
HTML
Embedded:
JSON
Turtle
Other:
CSV
JSON-LD
Faceted Browser
Sparql Endpoint
About:
Deletion (genetics)
An Entity of Type:
Thing
,
from Named Graph:
http://dbpedia.org
,
within Data Space:
dbpedia-live.demo.openlinksw.com
Mutation that removes a part of a DNA sequence
Property
Value
dbo:
description
genetica
(nl)
Störung einer Gensequenz
(de)
anomalía estructural cromosómica que consiste en la pérdida de un fragmento de ADN de un cromosoma
(es)
genetikai mutáció
(hu)
mutation som avlägsnar en del av DNA
(sv)
mutation that removes a part of a DNA sequence
(en)
tipo di mutazione cromosomica
(it)
хромосомные перестройки, при которых происходит потеря участка хромосомы
(ru)
mutacija, pri kateri pri do izgube dela zaporedja DNK
(sl)
돌연변이의 종류
(ko)
mutation génétique caractérisée par la perte de matériel génétique sur un chromosome
(fr)
dbo:
thumbnail
wiki-commons
:Special:FilePath/Deletion_of_chromosome_section.svg?width=300
dbo:
wikiPageWikiLink
dbr
:Saccharomyces_cerevisiae
dbr
:Indel
dbc
:Mutation
dbc
:Modification_of_genetic_information
dbr
:Chromosomal_crossover
dbr
:Unequal_crossing_over
dbr
:Meiosis
dbr
:Frameshift_mutation
dbr
:Chromosomal_inversion
dbr
:Medical_genetics
dbr
:Nomenclature
dbr
:Ape
dbr
:The_Cancer_Genome_Atlas
dbr
:Monkey
dbr
:DNA
dbr
:Genetics
dbr
:Protein
dbr
:Williams_syndrome
dbr
:Spinal_muscular_atrophy
dbr
:Cystic_fibrosis
dbr
:Infertility
dbr
:HCONDELs
dbr
:File:Human_karyotype_with_bands_and_sub-bands.png
dbr
:Delta_(letter)
dbr
:Null_allele
dbr
:Chromosome
dbr
:Tumor_suppressor_gene
dbr
:ΔF508
dbr
:Synapsis
dbr
:DNA_damage_(naturally_occurring)
dbr
:Mutation
dbr
:List_of_genetic_disorders
dbr
:Chromosomal_translocation
dbr
:Microdeletion_syndrome
dbr
:Mitochondrial_DNA
dbr
:Duchenne_muscular_dystrophy
dbr
:Insertion_(genetics)
dbr
:Prokaryotic
dbr
:Chromosomal_deletion_syndrome
dbr
:Eukaryotic
dbr
:Common_chimpanzee
dbr
:Nucleobase
dbr
:Nucleotides
dbr
:End-sequence_profiling
dbr
:International_System_for_Human_Cytogenomic_Nomenclature
dbr
:Codon
dbr
:Human_chromosome
dbr
:Cri_du_chat
dbr
:Genetic_disease
dbr
:File:Three_chromosomal_abnormalities_with_ISCN_nomenclature.png
dbr
:Chromosome_abnormalities
dbr
:Rad51
dbr
:Rad52
dbr
:File:Deletion_of_chromosome_section.svg
dbr
:Survival_motor_neuron
dbr
:Translation_(genetics)
dbp:
wikiPageUsesTemplate
dbt
:Commons_category
dbt
:Reflist
dbt
:Mutation
dbt
:Chromosomal_abnormalities
dbt
:Further
dbt
:Short_description
dct:
subject
dbc
:Mutation
dbc
:Modification_of_genetic_information
gold:
hypernym
dbr
:Mutation
rdfs:
label
Deletion (genetics)
(en)
حذف (وراثة)
(ar)
Deleció
(ca)
Delezio
(eu)
Deleción
(es)
Délétion
(fr)
Deletion
(de)
Delezione
(it)
欠失
(ja)
유전자 결실
(ko)
Delecja
(pl)
Deletie (genetica)
(nl)
Deleção
(pt)
Делеція (біологія)
(uk)
Делеция
(ru)
刪除 (遺傳學)
(zh)
owl:
sameAs
yago-res
:Deletion (genetics)
freebase
:Deletion (genetics)
wikidata
:Deletion (genetics)
dbpedia-it
:Deletion (genetics)
dbpedia-nl
:Deletion (genetics)
dbpedia-de
:Deletion (genetics)
dbpedia-fr
:Deletion (genetics)
dbpedia-tr
:Deletion (genetics)
dbpedia-zh
:Deletion (genetics)
dbpedia-ja
:Deletion (genetics)
dbpedia-pt
:Deletion (genetics)
dbpedia-es
:Deletion (genetics)
dbpedia-hu
:Deletion (genetics)
dbpedia-fa
:Deletion (genetics)
dbpedia-ru
:Deletion (genetics)
dbpedia-pl
:Deletion (genetics)
dbpedia-ko
:Deletion (genetics)
dbpedia-ca
:Deletion (genetics)
dbpedia-ar
:Deletion (genetics)
dbpedia-bs
:Deletion (genetics)
dbpedia-ckb
:Deletion (genetics)
dbpedia-eu
:Deletion (genetics)
dbpedia-gl
:Deletion (genetics)
dbpedia-hy
:Deletion (genetics)
dbpedia-ka
:Deletion (genetics)
dbpedia-kk
:Deletion (genetics)
dbpedia-ky
:Deletion (genetics)
dbpedia-la
:Deletion (genetics)
dbpedia-lt
:Deletion (genetics)
dbpedia-no
:Deletion (genetics)
dbpedia-sh
:Deletion (genetics)
dbpedia-sr
:Deletion (genetics)
dbpedia-th
:Deletion (genetics)
dbpedia-tl
:Deletion (genetics)
dbpedia-uk
:Deletion (genetics)
dbpedia-ur
:Deletion (genetics)
dbpedia-global
:Deletion (genetics)
dbr
:Deletion (genetics)
prov:
wasDerivedFrom
wikipedia-en
:Deletion_(genetics)?oldid=1279769256&ns=0
foaf:
depiction
wiki-commons
:Special:FilePath/Human_karyotype_with_bands_and_sub-bands.png
wiki-commons
:Special:FilePath/Deletion_of_chromosome_section.svg
wiki-commons
:Special:FilePath/Three_chromosomal_abnormalities_with_ISCN_nomenclature.png
foaf:
isPrimaryTopicOf
wikipedia-en
:Deletion_(genetics)
is
dbo:
wikiPageDisambiguates
of
dbr
:Deletion
is
dbo:
wikiPageRedirects
of
dbr
:Nucleotide_deletion
dbr
:Genetic_deletion
dbr
:Genetic_deletions
dbr
:Microdeletion
dbr
:Microdeletions
dbr
:Deletion_mutation
dbr
:Chromosomal_deletion
dbr
:Gene_deletion
dbr
:Point_deletion
dbr
:Sequence_deletion
dbr
:Single_deletion_mutation
is
dbo:
wikiPageWikiLink
of
dbr
:Archaeogenetics
dbr
:Lujan–Fryns_syndrome
dbr
:Bimolecular_fluorescence_complementation
dbr
:Jacobsen_syndrome
dbr
:Comparative_genomics
dbr
:Non-allelic_homologous_recombination
dbr
:Cycle_(gene)
dbr
:Haplogroup_A-L1085
dbr
:Mutagenesis_(molecular_biology_technique)
dbr
:Promoter_bashing
dbr
:Venetoclax
dbr
:Nuclear_protein_in_testis_gene
dbr
:Genocopy
dbr
:Lipofibromatosis
dbr
:XMEN_disease
dbr
:Induced_pluripotent_stem_cell
dbr
:Neural_crest
dbr
:Indel
dbr
:Seymour_Benzer
dbr
:Fukuyama_congenital_muscular_dystrophy
dbr
:Chromosomal_crossover
dbr
:Triple-stranded_DNA
dbr
:Clastogen
dbr
:Treacher_Collins_syndrome
dbr
:Corymbium
dbr
:Ocular_albinism_type_1
dbr
:Sequential_pattern_mining
dbr
:Mentha_gattefossei
dbr
:Somaclonal_variation
dbr
:Genome_instability
dbr
:Neuroligin
dbr
:Index_of_genetics_articles
dbr
:Outline_of_genetics
dbr
:Follicular_lymphoma
dbr
:Ring_chromosome_14_syndrome
dbr
:Koolen–De_Vries_syndrome
dbr
:Ty21a
dbr
:Autosomal_dominant_GTP_cyclohydrolase_I_deficiency
dbr
:Hypomyelination-congenital_cataract_syndrome
dbr
:Mandibulofacial_dysostosis-microcephaly_syndrome
dbr
:Pearson_syndrome
dbr
:Wolf–Hirschhorn_syndrome
dbr
:Microsatellite_instability
dbr
:Mentha_cervina
dbr
:Chromothripsis
dbr
:Chronic_lymphocytic_leukemia
dbr
:Genome-wide_association_study
dbr
:Recombinase-mediated_cassette_exchange
dbr
:Dominant_white
dbr
:Silent_mutation
dbr
:Arsenic_biochemistry
dbr
:Site-directed_mutagenesis
dbr
:Dicentric_chromosome
dbr
:TisB-IstR_toxin-antitoxin_system
dbr
:8-Oxo-2'-deoxyguanosine
dbr
:Human_genetics
dbr
:Isochromosome
dbr
:Werner_syndrome
dbr
:Biology
dbr
:Candida_albicans
dbr
:Craig_Venter
dbr
:Kodkod
dbr
:Pancreatic_cancer
dbr
:Gonadal_dysgenesis
dbr
:TATA_box
dbr
:Copy_number_variation
dbr
:Preimplantation_genetic_diagnosis
dbr
:Exonic_splicing_silencer
dbr
:Exonuclease_III
dbr
:FIE3_(ftz_instability_element_3′)_element
dbr
:Intermediate_mesoderm
dbr
:Liposarcoma
dbr
:Bicolor_cat
dbr
:Heritability_of_autism
dbr
:Cat_senses
dbr
:Cavea_tanguensis
dbr
:Glycerol_kinase_deficiency
dbr
:Index_of_HIV/AIDS-related_articles
dbr
:Index_of_molecular_biology_articles
dbr
:DNA
dbr
:Williams_syndrome
dbr
:2q37_monosomy
dbr
:Spinal_muscular_atrophy
dbr
:Aneuploidy
dbr
:BFAST
dbr
:ASPM_(gene)
dbr
:3q29_microdeletion_syndrome
dbr
:Blastic_plasmacytoid_dendritic_cell_neoplasm
dbr
:HCONDELs
dbr
:Race_and_genetics
dbr
:Liebenberg_syndrome
dbr
:Olduvai_domain
dbr
:He_Jiankui_affair
dbr
:ANNOVAR
dbr
:DAZ_protein_family
dbr
:Delta_(letter)
dbr
:Null_allele
dbr
:Autism_spectrum
dbr
:Chromosome
dbr
:Mixed_acid_fermentation
dbr
:Schizophrenia
dbr
:BRCA2
dbr
:Cyclic_nucleotide–gated_ion_channel
dbr
:Cystic_fibrosis_transmembrane_conductance_regulator
dbr
:Deletion
dbr
:Nuclease
dbr
:P16
dbr
:PTEN_(gene)
dbr
:Ribosomal_DNA
dbr
:1q21.1_deletion_syndrome
dbr
:Loss_of_heterozygosity
dbr
:Primary_effusion_lymphoma
dbr
:1q21.1_duplication_syndrome
dbr
:Facioscapulohumeral_muscular_dystrophy
dbr
:Fragile_X_syndrome
dbr
:Carcinogenesis
dbr
:Chromosome_abnormality
dbr
:Mutation
dbr
:Z-DNA
dbr
:Mycobacterium_leprae
dbr
:Heliotropium
dbr
:List_of_genetic_disorders
dbr
:Antineoplastic_resistance
dbr
:Cre-Lox_recombination
dbr
:Common_variable_immunodeficiency
dbr
:Index_of_biology_articles
dbr
:Base_excision_repair
dbr
:Mutation_breeding
dbr
:DECIPHER
dbr
:DNA_oxidation
dbr
:Pseudodominance
dbr
:Pseudolinkage
dbr
:Unicameral_bone_cyst
dbr
:Thomas_Szasz
dbr
:Genetic_variation
dbr
:Nucleic_acid_test
dbr
:Y-chromosomal_Adam
dbr
:Mutagen
dbr
:Promoter_activity
dbr
:Human_somatic_variation
dbr
:Börjeson–Forssman–Lehmann_syndrome
dbr
:Chromosomal_rearrangement
dbr
:Congenital_contractural_arachnodactyly
dbr
:Saethre–Chotzen_syndrome
dbr
:Genome_size
dbr
:Ancestral_reconstruction
dbr
:Splice_site_mutation
dbr
:Structural_variation
dbr
:Subtelomere
dbr
:T4_rII_system
dbr
:Paired-end_tag
dbr
:Plasmid
dbr
:Human_genetic_variation
dbr
:Suppressor_mutation
dbr
:Adaptive_evolution_in_the_human_genome
dbr
:Fibrous_hamartoma_of_infancy
dbr
:LETM1-like_protein_family
dbr
:Minor_histocompatibility_antigen
dbr
:MtDNA_control_region
dbr
:Spinal_muscular_atrophy_with_progressive_myoclonic_epilepsy
dbr
:Uterus-like_mass
dbr
:VPS13B
dbr
:Microdeletion_syndrome
dbr
:Cell-free_fetal_DNA
dbr
:Gymnarrhenoideae
dbr
:Calponin_1
dbr
:Tree_alignment
dbr
:Molecular_evolution
dbr
:Deletion_mapping
dbr
:Somatic_mutation_and_recombination_tests
dbr
:Rhodococcus_equi
dbr
:Inverted_repeat
dbr
:Insertion_(genetics)
dbr
:Fusion_gene
dbr
:SARS-CoV-2_Alpha_variant
dbr
:Extranuclear_inheritance
dbr
:Conserved_sequence
dbr
:Chromatin_bridge
dbr
:Complement_receptor_1
dbr
:Mammary-type_myofibroblastoma
dbr
:Methylglutaconyl-CoA_hydratase
dbr
:Miller–Dieker_syndrome
dbr
:Toxin-antitoxin_system
dbr
:Coding_region
dbr
:Computational_phylogenetics
dbr
:5′_flanking_region
dbr
:Gap_penalty
dbr
:Black_squirrel
dbr
:GLUT1
dbr
:Willy_A._Flegel
dbr
:Y_linkage
dbr
:1q21.1_copy_number_variations
dbr
:Extranodal_NK/T-cell_lymphoma,_nasal_type
dbr
:Aromatase_excess_syndrome
dbr
:Controversies_in_autism
dbr
:Dermatopathia_pigmentosa_reticularis
dbr
:Ichthyosis_prematurity_syndrome
dbr
:Lorna_Casselton
dbr
:Low-grade_fibromyxoid_sarcoma
dbr
:Sib_RNA
dbr
:Sickle_cell_nephropathy
dbr
:Wingless_localisation_element_3_(WLE3)
dbr
:Alveolar_capillary_dysplasia
dbr
:Genetic_imbalance
dbr
:Genetically_modified_virus
dbr
:Molecular_Inversion_Probe
dbr
:Molecular_drive
dbr
:Molecular_lesion
dbr
:Chromosomal_deletion_syndrome
dbr
:Hereditary_diffuse_leukoencephalopathy_with_spheroids
dbr
:Dysfibrinogenemia
dbr
:Restriction_landmark_genomic_scanning
dbr
:Retroviral_psi_packaging_element
dbr
:Insulated_neighborhood
dbr
:Ruff_(bird)
dbr
:In_situ_lymphoid_neoplasia
dbr
:Lipofibromatosis-like_neural_tumor
dbr
:Angiofibroma_of_soft_tissue
dbr
:Cellular_angiofibroma
dbr
:Siglec
dbr
:Somatic_recombination
dbr
:Pediatric-type_follicular_lymphoma
dbr
:Primary_testicular_diffuse_large_B-cell_lymphoma
dbr
:Vel_blood_group
dbr
:Biological_tests_of_necessity_and_sufficiency
dbr
:Virtual_karyotype
dbr
:R‑banding
dbr
:BEND2_(protein)
dbr
:C3orf70
dbr
:FIP1L1
dbr
:NUBPL
dbr
:SERPINA2
dbr
:Phenol_sulfur_transferase_deficiency
dbr
:Double-strand_break_repair_model
dbr
:Woodhouse–Sakati_syndrome
dbr
:GATA2_deficiency
dbr
:Ring_chromosome_22
dbr
:Monomorphic_epitheliotropic_intestinal_T_cell_lymphoma
dbr
:Nodular_fasciitis
dbr
:CMAH
dbr
:COA7
dbr
:DIP2A
dbr
:GATA2
dbr
:GATA3
dbr
:LETM1
dbr
:MAP2K1
dbr
:MTAP
dbr
:OPN1LW
dbr
:PDGFRB
dbr
:PITX1
dbr
:SETD2
dbr
:SURF1
dbr
:TBX4
dbr
:USH1C
dbr
:USP6
dbr
:PRP36
dbr
:CLCN5
dbr
:COX10
dbr
:PAK5
dbr
:Sister_chromatid_exchange
dbr
:Prime_editing
dbr
:Filippi_syndrome
dbr
:Dicarboxylic_aminoaciduria
dbr
:Evolving_digital_ecological_network
dbr
:Gymnarrhena
dbr
:Worm_bagging
dbr
:Egg_predation
dbr
:Keratin_5
dbr
:Oxoguanine_glycosylase
dbr
:SLC22A5
dbr
:Porocarcinoma
dbr
:End-sequence_profiling
dbr
:Off-target_genome_editing
dbr
:Streamlining_theory
dbr
:Prescopranone
dbr
:Sclerosing_epithelioid_fibrosarcoma
dbr
:17q12_microdeletion_syndrome
dbr
:Eremothecium_gossypii
dbr
:Aldred_syndrome
dbr
:Infectious_bronchitis_virus_D-RNA
dbr
:PGM3_deficiency
dbr
:Dysosteosclerosis
dbr
:Canine_coronavirus_HuPn-2018
dbr
:FET_protein_family
dbr
:Glossary_of_genetics
dbr
:2022_in_paleomammalogy
dbr
:Multiple_sclerosis_research
dbr
:Nucleotide_deletion
dbr
:Glossary_of_genetics_(0–L)
dbr
:Genetic_deletion
dbr
:Genetic_deletions
dbr
:Microdeletion
dbr
:Microdeletions
dbr
:Dock8
dbr
:Deletion_mutation
dbr
:Chromosomal_deletion
dbr
:Gene_deletion
dbr
:Point_deletion
dbr
:Sequence_deletion
dbr
:Single_deletion_mutation
is
foaf:
primaryTopic
of
wikipedia-en
:Deletion_(genetics)
This content was extracted from
Wikipedia
and is licensed under the
Creative Commons Attribution-ShareAlike 4.0 International