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- source_evidence_literature type ECO_0000212 NP734288.RArYxdxNnZ3IF3UuzFfDxT1AgU4dK4d9eZEZyk0GImIi0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP734288.RArYxdxNnZ3IF3UuzFfDxT1AgU4dK4d9eZEZyk0GImIi0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP734288.RArYxdxNnZ3IF3UuzFfDxT1AgU4dK4d9eZEZyk0GImIi0130_provenance.
- NP734288.RArYxdxNnZ3IF3UuzFfDxT1AgU4dK4d9eZEZyk0GImIi0130_assertion description "[To extend these results we searched for mutations of ASXL1 in a series of chronic myelomonocytic leukaemias, a disease classified as MDS/Myeloproliferative disorder, and found mutations in 17 out of 39 patients (43%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734288.RArYxdxNnZ3IF3UuzFfDxT1AgU4dK4d9eZEZyk0GImIi0130_provenance.
- NP734288.RArYxdxNnZ3IF3UuzFfDxT1AgU4dK4d9eZEZyk0GImIi0130_assertion evidence source_evidence_literature NP734288.RArYxdxNnZ3IF3UuzFfDxT1AgU4dK4d9eZEZyk0GImIi0130_provenance.
- NP734288.RArYxdxNnZ3IF3UuzFfDxT1AgU4dK4d9eZEZyk0GImIi0130_assertion SIO_000772 19388938 NP734288.RArYxdxNnZ3IF3UuzFfDxT1AgU4dK4d9eZEZyk0GImIi0130_provenance.
- NP734288.RArYxdxNnZ3IF3UuzFfDxT1AgU4dK4d9eZEZyk0GImIi0130_assertion wasDerivedFrom befree-2016 NP734288.RArYxdxNnZ3IF3UuzFfDxT1AgU4dK4d9eZEZyk0GImIi0130_provenance.
- NP734288.RArYxdxNnZ3IF3UuzFfDxT1AgU4dK4d9eZEZyk0GImIi0130_assertion wasGeneratedBy ECO_0000203 NP734288.RArYxdxNnZ3IF3UuzFfDxT1AgU4dK4d9eZEZyk0GImIi0130_provenance.
- befree-2016 importedOn "2016-02-19" NP734288.RArYxdxNnZ3IF3UuzFfDxT1AgU4dK4d9eZEZyk0GImIi0130_provenance.