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- source_evidence_literature type ECO_0000212 NP1319767.RA89RkT3HGVOr12bdevJVd9AlTv7wN7pfORlXqBLMWc68130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1319767.RA89RkT3HGVOr12bdevJVd9AlTv7wN7pfORlXqBLMWc68130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1319767.RA89RkT3HGVOr12bdevJVd9AlTv7wN7pfORlXqBLMWc68130_provenance.
- NP1319767.RA89RkT3HGVOr12bdevJVd9AlTv7wN7pfORlXqBLMWc68130_assertion description "[We found only one mutation of the N-ras gene that was a 2-bp substitution of GGT(Gly) to GTC(Val) at codon 13 among 22 t(1;19)-ALL cases and five cell lines.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1319767.RA89RkT3HGVOr12bdevJVd9AlTv7wN7pfORlXqBLMWc68130_provenance.
- NP1319767.RA89RkT3HGVOr12bdevJVd9AlTv7wN7pfORlXqBLMWc68130_assertion evidence source_evidence_literature NP1319767.RA89RkT3HGVOr12bdevJVd9AlTv7wN7pfORlXqBLMWc68130_provenance.
- NP1319767.RA89RkT3HGVOr12bdevJVd9AlTv7wN7pfORlXqBLMWc68130_assertion SIO_000772 7727782 NP1319767.RA89RkT3HGVOr12bdevJVd9AlTv7wN7pfORlXqBLMWc68130_provenance.
- NP1319767.RA89RkT3HGVOr12bdevJVd9AlTv7wN7pfORlXqBLMWc68130_assertion wasDerivedFrom befree-2016 NP1319767.RA89RkT3HGVOr12bdevJVd9AlTv7wN7pfORlXqBLMWc68130_provenance.
- NP1319767.RA89RkT3HGVOr12bdevJVd9AlTv7wN7pfORlXqBLMWc68130_assertion wasGeneratedBy ECO_0000203 NP1319767.RA89RkT3HGVOr12bdevJVd9AlTv7wN7pfORlXqBLMWc68130_provenance.
- befree-2016 importedOn "2016-02-19" NP1319767.RA89RkT3HGVOr12bdevJVd9AlTv7wN7pfORlXqBLMWc68130_provenance.