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- source_evidence_literature type ECO_0000212 NP781348.RAyB78L_2dhFZGT994-ZgTUD0Ayse3Y4wKfihAxQcfoIE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP781348.RAyB78L_2dhFZGT994-ZgTUD0Ayse3Y4wKfihAxQcfoIE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP781348.RAyB78L_2dhFZGT994-ZgTUD0Ayse3Y4wKfihAxQcfoIE130_provenance.
- NP781348.RAyB78L_2dhFZGT994-ZgTUD0Ayse3Y4wKfihAxQcfoIE130_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." NP781348.RAyB78L_2dhFZGT994-ZgTUD0Ayse3Y4wKfihAxQcfoIE130_provenance.
- NP781348.RAyB78L_2dhFZGT994-ZgTUD0Ayse3Y4wKfihAxQcfoIE130_assertion evidence source_evidence_literature NP781348.RAyB78L_2dhFZGT994-ZgTUD0Ayse3Y4wKfihAxQcfoIE130_provenance.
- NP781348.RAyB78L_2dhFZGT994-ZgTUD0Ayse3Y4wKfihAxQcfoIE130_assertion SIO_000772 23643325 NP781348.RAyB78L_2dhFZGT994-ZgTUD0Ayse3Y4wKfihAxQcfoIE130_provenance.
- NP781348.RAyB78L_2dhFZGT994-ZgTUD0Ayse3Y4wKfihAxQcfoIE130_assertion wasDerivedFrom befree-20150227 NP781348.RAyB78L_2dhFZGT994-ZgTUD0Ayse3Y4wKfihAxQcfoIE130_provenance.
- NP781348.RAyB78L_2dhFZGT994-ZgTUD0Ayse3Y4wKfihAxQcfoIE130_assertion wasGeneratedBy ECO_0000203 NP781348.RAyB78L_2dhFZGT994-ZgTUD0Ayse3Y4wKfihAxQcfoIE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP781348.RAyB78L_2dhFZGT994-ZgTUD0Ayse3Y4wKfihAxQcfoIE130_provenance.