|Dataset||DISEASES Text-mining Gene-Disease Assocation Evidence Scores|
|Category||disease or phenotype associations|
|Description||A severe combined immunodeficiency that is the result of a mutation on Chromosome 6 RAG1 gene involving genetic rearrangement of both the T- and B-lymphocyte receptor genes. (Human Disease Ontology, DOID_0060011)|
|Downloads & Tools|
1 genes co-occuring with the disease recombinase activating gene 1 deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
|RAG1||recombination activating gene 1||1.05597|