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- source_evidence_literature type ECO_0000212 NP597479.RAE0TEM7z3I-om4RbOBGcsRtYma8BdPw26IM4Y-dMIcqc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP597479.RAE0TEM7z3I-om4RbOBGcsRtYma8BdPw26IM4Y-dMIcqc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP597479.RAE0TEM7z3I-om4RbOBGcsRtYma8BdPw26IM4Y-dMIcqc130_provenance.
- NP597479.RAE0TEM7z3I-om4RbOBGcsRtYma8BdPw26IM4Y-dMIcqc130_assertion description "[These in vitro studies have demonstrated that the proliferation is characterized by a unique chromosomal abnormality, the 5q35bp usually associated with a t(2;5) translocation generating a fusion gene NPM/ALK and the subsequent translation of p80 protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597479.RAE0TEM7z3I-om4RbOBGcsRtYma8BdPw26IM4Y-dMIcqc130_provenance.
- NP597479.RAE0TEM7z3I-om4RbOBGcsRtYma8BdPw26IM4Y-dMIcqc130_assertion evidence source_evidence_literature NP597479.RAE0TEM7z3I-om4RbOBGcsRtYma8BdPw26IM4Y-dMIcqc130_provenance.
- NP597479.RAE0TEM7z3I-om4RbOBGcsRtYma8BdPw26IM4Y-dMIcqc130_assertion SIO_000772 9561912 NP597479.RAE0TEM7z3I-om4RbOBGcsRtYma8BdPw26IM4Y-dMIcqc130_provenance.
- NP597479.RAE0TEM7z3I-om4RbOBGcsRtYma8BdPw26IM4Y-dMIcqc130_assertion wasDerivedFrom befree-20150227 NP597479.RAE0TEM7z3I-om4RbOBGcsRtYma8BdPw26IM4Y-dMIcqc130_provenance.
- NP597479.RAE0TEM7z3I-om4RbOBGcsRtYma8BdPw26IM4Y-dMIcqc130_assertion wasGeneratedBy ECO_0000203 NP597479.RAE0TEM7z3I-om4RbOBGcsRtYma8BdPw26IM4Y-dMIcqc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP597479.RAE0TEM7z3I-om4RbOBGcsRtYma8BdPw26IM4Y-dMIcqc130_provenance.