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- source_evidence_literature type ECO_0000212 NP1074846.RAHPY1XfPrIBaea06-MwQpy599GqcjkheISt7jCztofJo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1074846.RAHPY1XfPrIBaea06-MwQpy599GqcjkheISt7jCztofJo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1074846.RAHPY1XfPrIBaea06-MwQpy599GqcjkheISt7jCztofJo130_provenance.
- NP1074846.RAHPY1XfPrIBaea06-MwQpy599GqcjkheISt7jCztofJo130_assertion description "[Focusing on cytogenetic aberrations most commonly found in MDS, we retrospectively genotyped 566 MDS/AML patients carrying -5/del(5q), -7/del(7q), +8, del(20q) and -Y.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1074846.RAHPY1XfPrIBaea06-MwQpy599GqcjkheISt7jCztofJo130_provenance.
- NP1074846.RAHPY1XfPrIBaea06-MwQpy599GqcjkheISt7jCztofJo130_assertion evidence source_evidence_literature NP1074846.RAHPY1XfPrIBaea06-MwQpy599GqcjkheISt7jCztofJo130_provenance.
- NP1074846.RAHPY1XfPrIBaea06-MwQpy599GqcjkheISt7jCztofJo130_assertion SIO_000772 23643325 NP1074846.RAHPY1XfPrIBaea06-MwQpy599GqcjkheISt7jCztofJo130_provenance.
- NP1074846.RAHPY1XfPrIBaea06-MwQpy599GqcjkheISt7jCztofJo130_assertion wasDerivedFrom befree-2016 NP1074846.RAHPY1XfPrIBaea06-MwQpy599GqcjkheISt7jCztofJo130_provenance.
- NP1074846.RAHPY1XfPrIBaea06-MwQpy599GqcjkheISt7jCztofJo130_assertion wasGeneratedBy ECO_0000203 NP1074846.RAHPY1XfPrIBaea06-MwQpy599GqcjkheISt7jCztofJo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1074846.RAHPY1XfPrIBaea06-MwQpy599GqcjkheISt7jCztofJo130_provenance.