Human Genome Variation Society standards
E1589493
UNEXPLORED
Human Genome Variation Society standards are internationally recognized guidelines for the consistent nomenclature and reporting of genetic sequence variants in human DNA.
All labels observed (1)
| Label | Occurrences |
|---|---|
| Human Genome Variation Society standards canonical | 1 |
How this entity was disambiguated
This entity first appeared as the object of triple T23467057 — 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: Human Genome Variation Society standards Context triple: [ClinVar, usesStandard, Human Genome Variation Society standards]
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A.
Personal Genome Project
The Personal Genome Project is a pioneering open-science initiative that publicly shares the genomic and health data of volunteers to advance research and understanding of human genetics.
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B.
National Institute of Biomedical Genomics
The National Institute of Biomedical Genomics is an Indian research and training institution dedicated to advancing biomedical genomics, including human disease genomics and public health genomics.
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C.
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.
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D.
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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E.
Center of Excellence in Genomic Medicine Research
The Center of Excellence in Genomic Medicine Research is a specialized research institute at King Abdulaziz University focused on advancing genomic science and its applications in medicine and healthcare.
- 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: Human Genome Variation Society standards Target entity description: Human Genome Variation Society standards are internationally recognized guidelines for the consistent nomenclature and reporting of genetic sequence variants in human DNA.
-
A.
Personal Genome Project
The Personal Genome Project is a pioneering open-science initiative that publicly shares the genomic and health data of volunteers to advance research and understanding of human genetics.
-
B.
National Institute of Biomedical Genomics
The National Institute of Biomedical Genomics is an Indian research and training institution dedicated to advancing biomedical genomics, including human disease genomics and public health genomics.
-
C.
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.
-
D.
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.
-
E.
Center of Excellence in Genomic Medicine Research
The Center of Excellence in Genomic Medicine Research is a specialized research institute at King Abdulaziz University focused on advancing genomic science and its applications in medicine and healthcare.
- F. None of above. chosen
Referenced by (1)
Full triples — surface form annotated when it differs from this entity's canonical label.
subject linked to:
ClinVar database