Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP286388.RAOnxn5xOaGTBPw0Ha7lD6WtUx7aPAKIEZMUeo3Ir_QpM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP286388.RAOnxn5xOaGTBPw0Ha7lD6WtUx7aPAKIEZMUeo3Ir_QpM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP286388.RAOnxn5xOaGTBPw0Ha7lD6WtUx7aPAKIEZMUeo3Ir_QpM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP286388.RAOnxn5xOaGTBPw0Ha7lD6WtUx7aPAKIEZMUeo3Ir_QpM130_provenance.
- NP286388.RAOnxn5xOaGTBPw0Ha7lD6WtUx7aPAKIEZMUeo3Ir_QpM130_assertion description "[We identified additional molecular aberrations in 24/27 (89%) patients with advanced SM (SM-AHNMD, 5/5; aggressive SM/mast cell leukemia, 19/22) whereas only 3/12 (25%) indolent SM/smoldering SM patients carried one additional mutation each (U2AF1, SETBP1, CBL) (P < .001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP286388.RAOnxn5xOaGTBPw0Ha7lD6WtUx7aPAKIEZMUeo3Ir_QpM130_provenance.
- NP286388.RAOnxn5xOaGTBPw0Ha7lD6WtUx7aPAKIEZMUeo3Ir_QpM130_assertion evidence source_evidence_literature NP286388.RAOnxn5xOaGTBPw0Ha7lD6WtUx7aPAKIEZMUeo3Ir_QpM130_provenance.
- NP286388.RAOnxn5xOaGTBPw0Ha7lD6WtUx7aPAKIEZMUeo3Ir_QpM130_assertion SIO_000772 23958953 NP286388.RAOnxn5xOaGTBPw0Ha7lD6WtUx7aPAKIEZMUeo3Ir_QpM130_provenance.
- NP286388.RAOnxn5xOaGTBPw0Ha7lD6WtUx7aPAKIEZMUeo3Ir_QpM130_assertion wasDerivedFrom befree-20150227 NP286388.RAOnxn5xOaGTBPw0Ha7lD6WtUx7aPAKIEZMUeo3Ir_QpM130_provenance.
- NP286388.RAOnxn5xOaGTBPw0Ha7lD6WtUx7aPAKIEZMUeo3Ir_QpM130_assertion wasGeneratedBy ECO_0000203 NP286388.RAOnxn5xOaGTBPw0Ha7lD6WtUx7aPAKIEZMUeo3Ir_QpM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP286388.RAOnxn5xOaGTBPw0Ha7lD6WtUx7aPAKIEZMUeo3Ir_QpM130_provenance.