Properties (60)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
family
|
| gptkbp:associatedWith |
C75 family
disease phenotypes C76_protein |
| gptkbp:characterizedBy |
specific mutations
|
| gptkbp:countryOfOrigin |
common ancestor
|
| gptkbp:exhibits |
gene duplication
|
| gptkbp:function |
biological regulation
|
| gptkbp:hasCollaboratedWith |
international research projects
|
| gptkbp:hasExhibition |
C77_family
|
| gptkbp:hasImpactOn |
healthcare
|
| gptkbp:hasMember |
C76-1
C76-2 C76-3 C76-4 C76-5 |
| gptkbp:hasResearchInterest |
gene therapy
|
| https://www.w3.org/2000/01/rdf-schema#label |
C76 family
|
| gptkbp:influences |
cellular processes
|
| gptkbp:involvedIn |
cell signaling
|
| gptkbp:is_evaluated_by |
various tissues
|
| gptkbp:isActiveIn |
bioinformatics
|
| gptkbp:isAssociatedWith |
biomarkers
lifestyle diseases |
| gptkbp:isAvenueFor |
functional genomics
|
| gptkbp:isCharacterizedBy |
functional assays
|
| gptkbp:isDescribedAs |
scientific literature
|
| gptkbp:isDocumentedIn |
genetic databases
|
| gptkbp:isExaminedBy |
clinical trials
therapeutic efficacy drug resistance therapeutic potential |
| gptkbp:isExploredIn |
human studies
|
| gptkbp:isInvolvedIn |
cellular metabolism
protein interactions |
| gptkbp:isLinkedTo |
environmental factors
therapeutic targets |
| gptkbp:isPartOf |
genetic engineering
genomic studies molecular genetics genetic mapping C76_group |
| gptkbp:isReferencedIn |
academic publications
|
| gptkbp:isRelatedTo |
pharmacogenomics
|
| gptkbp:isStudiedIn |
population genetics
cancer research evolutionary relationships |
| gptkbp:isUtilizedFor |
animal models
therapeutic interventions |
| gptkbp:isUtilizedIn |
diagnostic tests
|
| gptkbp:linkedTo |
metabolic pathways
|
| gptkbp:locatedIn |
1990s
human genome |
| gptkbp:notableFeature |
evolutionary biology
|
| gptkbp:recognizedBy |
gene sequencing
|
| gptkbp:relatedTo |
C76_gene
|
| gptkbp:research |
molecular biology
|
| gptkbp:researchFocus |
genetic disorders
|
| gptkbp:subject |
natural selection
|
| gptkbp:winner |
mutation
|