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- source_evidence_literature type ECO_0000212 NP266560.RAsdek2A7hCNCqx90RauXlwRQJ8jp_6N0RwH9aAiZB-VU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP266560.RAsdek2A7hCNCqx90RauXlwRQJ8jp_6N0RwH9aAiZB-VU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP266560.RAsdek2A7hCNCqx90RauXlwRQJ8jp_6N0RwH9aAiZB-VU130_provenance.
- NP266560.RAsdek2A7hCNCqx90RauXlwRQJ8jp_6N0RwH9aAiZB-VU130_assertion description "[Our objective in this study was to evaluate the genetic alterations in pediatric GBM (age < or = 18 years) with special reference to p53, p16, and p27 protein expression, alterations of the epidermal growth factor receptor (EGFR), and deletion of the phosphate and tensin homolog gene (PTEN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP266560.RAsdek2A7hCNCqx90RauXlwRQJ8jp_6N0RwH9aAiZB-VU130_provenance.
- NP266560.RAsdek2A7hCNCqx90RauXlwRQJ8jp_6N0RwH9aAiZB-VU130_assertion evidence source_evidence_literature NP266560.RAsdek2A7hCNCqx90RauXlwRQJ8jp_6N0RwH9aAiZB-VU130_provenance.
- NP266560.RAsdek2A7hCNCqx90RauXlwRQJ8jp_6N0RwH9aAiZB-VU130_assertion SIO_000772 18981259 NP266560.RAsdek2A7hCNCqx90RauXlwRQJ8jp_6N0RwH9aAiZB-VU130_provenance.
- NP266560.RAsdek2A7hCNCqx90RauXlwRQJ8jp_6N0RwH9aAiZB-VU130_assertion wasDerivedFrom befree-20140225 NP266560.RAsdek2A7hCNCqx90RauXlwRQJ8jp_6N0RwH9aAiZB-VU130_provenance.
- NP266560.RAsdek2A7hCNCqx90RauXlwRQJ8jp_6N0RwH9aAiZB-VU130_assertion wasGeneratedBy ECO_0000203 NP266560.RAsdek2A7hCNCqx90RauXlwRQJ8jp_6N0RwH9aAiZB-VU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP266560.RAsdek2A7hCNCqx90RauXlwRQJ8jp_6N0RwH9aAiZB-VU130_provenance.