Statements (87)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:academic
|
| gptkbp:appliesTo |
forensic science
personalized medicine ancestry analysis |
| gptkbp:focusesOn |
population genetics
genetic counseling genetic testing gene therapy epigenetics hereditary diseases genetic variation chromosomal abnormalities gene mapping |
| gptkbp:hasConcept |
gptkb:Mendelian_inheritance
gptkb:SNP gptkb:gene pharmacogenomics genetic disorder genetic epidemiology genetic counseling autosomal dominant chromosomal band epistasis gene therapy imprinting genetic drift genetic susceptibility autosomal recessive mitochondrial inheritance phenotype 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 |
| https://www.w3.org/2000/01/rdf-schema#label |
Human Genetics
|
| 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
|