DISEASES

Disease-gene associations mined from literature

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Human genes for glioblastoma mesenchymal subtype

Glioblastoma mesenchymal subtype [DOID:0050805]

A glioblastoma that is characterized by the most frequent number of mutation of the Neurofibromin 1 gene.

Synonyms:  glioblastoma mesenchymal subtype,  DOID:0050805,  glioblastoma mesenchymal subtypes

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.