Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418924.RAKQnlsrf3ybNCLXHGtw1RjrXNoSAWIfLj5FU5q1GsL-Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418924.RAKQnlsrf3ybNCLXHGtw1RjrXNoSAWIfLj5FU5q1GsL-Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418924.RAKQnlsrf3ybNCLXHGtw1RjrXNoSAWIfLj5FU5q1GsL-Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418924.RAKQnlsrf3ybNCLXHGtw1RjrXNoSAWIfLj5FU5q1GsL-Y130_provenance.
- NP418924.RAKQnlsrf3ybNCLXHGtw1RjrXNoSAWIfLj5FU5q1GsL-Y130_assertion description "[These findings confirm that germline GATA2 mutations predispose to familial myelodysplastic syndrome/acute myeloid leukemia, and that monosomy 7 and ASXL1 mutations may be recurrent secondary genetic abnormalities triggering overt malignancy in these families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418924.RAKQnlsrf3ybNCLXHGtw1RjrXNoSAWIfLj5FU5q1GsL-Y130_provenance.
- NP418924.RAKQnlsrf3ybNCLXHGtw1RjrXNoSAWIfLj5FU5q1GsL-Y130_assertion evidence source_evidence_literature NP418924.RAKQnlsrf3ybNCLXHGtw1RjrXNoSAWIfLj5FU5q1GsL-Y130_provenance.
- NP418924.RAKQnlsrf3ybNCLXHGtw1RjrXNoSAWIfLj5FU5q1GsL-Y130_assertion SIO_000772 22271902 NP418924.RAKQnlsrf3ybNCLXHGtw1RjrXNoSAWIfLj5FU5q1GsL-Y130_provenance.
- NP418924.RAKQnlsrf3ybNCLXHGtw1RjrXNoSAWIfLj5FU5q1GsL-Y130_assertion wasDerivedFrom befree-20150227 NP418924.RAKQnlsrf3ybNCLXHGtw1RjrXNoSAWIfLj5FU5q1GsL-Y130_provenance.
- NP418924.RAKQnlsrf3ybNCLXHGtw1RjrXNoSAWIfLj5FU5q1GsL-Y130_assertion wasGeneratedBy ECO_0000203 NP418924.RAKQnlsrf3ybNCLXHGtw1RjrXNoSAWIfLj5FU5q1GsL-Y130_provenance.
- befree-20150227 importedOn "2015-02-27" NP418924.RAKQnlsrf3ybNCLXHGtw1RjrXNoSAWIfLj5FU5q1GsL-Y130_provenance.