dbSNP
E1589860
UNEXPLORED
dbSNP is a public NCBI database that catalogs single nucleotide polymorphisms and other small genetic variants across diverse organisms for use in genetic and genomic research.
All labels observed (3)
How this entity was disambiguated
This entity first appeared as the object of triple T23466496 — resolving that mention is where its identity was fixed. The disambiguator weighed these candidate entities and picked the highlighted one (or “None”, minting a new entity). This is how homonymy is resolved: the same surface form can point to different entities.
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: dbSNP Context triple: [dbVar, integratedWith, dbSNP]
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A.
Ensembl
Ensembl is a comprehensive genome annotation and browsing platform that provides detailed, regularly updated genomic data for a wide range of species.
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B.
ClinVar database
The ClinVar database is a public archive that aggregates information about the clinical significance of genetic variants and their relationships to human health.
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C.
NCBI MedGen database
The NCBI MedGen database is a curated resource that aggregates information on human medical genetics, including diseases, phenotypes, and related genomic data, to support clinical and research applications.
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D.
NCBI Gene database
The NCBI Gene database is a comprehensive public resource that provides curated information on genes from multiple organisms, including their sequences, functions, genomic context, and related literature.
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E.
Genetic Testing Registry
The Genetic Testing Registry is an NIH-maintained public resource that provides detailed information about genetic tests, their purposes, methodologies, and associated conditions.
- F. None of above. chosen
- G. Unsure - the case is ambiguous/there is not enough information to decide.
NED2
Entity disambiguation (via description)
gpt-5-mini-2025-08-07
Target entity: dbSNP Target entity description: dbSNP is a public NCBI database that catalogs single nucleotide polymorphisms and other small genetic variants across diverse organisms for use in genetic and genomic research.
-
A.
Ensembl
Ensembl is a comprehensive genome annotation and browsing platform that provides detailed, regularly updated genomic data for a wide range of species.
-
B.
ClinVar database
The ClinVar database is a public archive that aggregates information about the clinical significance of genetic variants and their relationships to human health.
-
C.
NCBI MedGen database
The NCBI MedGen database is a curated resource that aggregates information on human medical genetics, including diseases, phenotypes, and related genomic data, to support clinical and research applications.
-
D.
NCBI Gene database
The NCBI Gene database is a comprehensive public resource that provides curated information on genes from multiple organisms, including their sequences, functions, genomic context, and related literature.
-
E.
Genetic Testing Registry
The Genetic Testing Registry is an NIH-maintained public resource that provides detailed information about genetic tests, their purposes, methodologies, and associated conditions.
- F. None of above. chosen
Referenced by (4)
Full triples — surface form annotated when it differs from this entity's canonical label.