Statements (87)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:academic
|
| gptkbp:appliesTo |
forensic science
personalized medicine ancestry analysis |
| gptkbp:focusesOn |
gptkb:gene_therapy
gptkb:genetic_variation population genetics genetic counseling genetic testing epigenetics hereditary diseases chromosomal abnormalities gene mapping |
| gptkbp:hasConcept |
gptkb:gene_therapy
gptkb:chromosomal_band gptkb:genetic_disorder gptkb:phenotype gptkb:Mendelian_inheritance gptkb:SNP gptkb:gene pharmacogenomics genetic epidemiology genetic counseling autosomal dominant epistasis imprinting genetic drift genetic susceptibility autosomal recessive mitochondrial inheritance carrier screening consanguinity genetic screening copy number variation locus newborn screening founder effect uniparental disomy prenatal diagnosis gene-environment interaction penetrance genetic heterogeneity pleiotropy expressivity trinucleotide repeat expansion X-linked inheritance genetic anticipation genetic isolation genetic mosaicism linkage disequilibrium multifactorial inheritance |
| gptkbp:hasSubfield |
cytogenetics
genomics medical genetics population genetics clinical genetics genetic epidemiology molecular genetics epigenetics behavioral genetics pharmacogenetics |
| gptkbp:importantFor |
public health
personalized medicine evolutionary studies forensic identification ancestry tracing developing gene therapies identifying disease risk understanding genetic disorders |
| gptkbp:relatedTo |
gptkb:medicine
genetics genomics molecular biology |
| gptkbp:studies |
inheritance in humans
|
| gptkbp:uses |
gptkb:polymerase_chain_reaction
CRISPR gene editing cytogenetics bioinformatics DNA sequencing genome-wide association studies karyotyping microarray analysis genetic linkage analysis pedigree analysis |
| gptkbp:bfsParent |
gptkb:R._Ruggles_Gates
|
| gptkbp:bfsLayer |
6
|
| https://www.w3.org/2000/01/rdf-schema#label |
Human Genetics
|