Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP734288.RArYxdxNnZ3IF3UuzFfDxT1AgU4dK4d9eZEZyk0GImIi0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP734288.RArYxdxNnZ3IF3UuzFfDxT1AgU4dK4d9eZEZyk0GImIi0130_assertion type Assertion NP734288.RArYxdxNnZ3IF3UuzFfDxT1AgU4dK4d9eZEZyk0GImIi0130_head.
- 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.