Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1103673.RA3I4i_OuK8_RCvwco1jv_GiC1jaemFi0hAMBHRoEM7RQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1103673.RA3I4i_OuK8_RCvwco1jv_GiC1jaemFi0hAMBHRoEM7RQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1103673.RA3I4i_OuK8_RCvwco1jv_GiC1jaemFi0hAMBHRoEM7RQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1103673.RA3I4i_OuK8_RCvwco1jv_GiC1jaemFi0hAMBHRoEM7RQ130_provenance.
- NP1103673.RA3I4i_OuK8_RCvwco1jv_GiC1jaemFi0hAMBHRoEM7RQ130_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." NP1103673.RA3I4i_OuK8_RCvwco1jv_GiC1jaemFi0hAMBHRoEM7RQ130_provenance.
- NP1103673.RA3I4i_OuK8_RCvwco1jv_GiC1jaemFi0hAMBHRoEM7RQ130_assertion evidence source_evidence_literature NP1103673.RA3I4i_OuK8_RCvwco1jv_GiC1jaemFi0hAMBHRoEM7RQ130_provenance.
- NP1103673.RA3I4i_OuK8_RCvwco1jv_GiC1jaemFi0hAMBHRoEM7RQ130_assertion SIO_000772 23958953 NP1103673.RA3I4i_OuK8_RCvwco1jv_GiC1jaemFi0hAMBHRoEM7RQ130_provenance.
- NP1103673.RA3I4i_OuK8_RCvwco1jv_GiC1jaemFi0hAMBHRoEM7RQ130_assertion wasDerivedFrom befree-2016 NP1103673.RA3I4i_OuK8_RCvwco1jv_GiC1jaemFi0hAMBHRoEM7RQ130_provenance.
- NP1103673.RA3I4i_OuK8_RCvwco1jv_GiC1jaemFi0hAMBHRoEM7RQ130_assertion wasGeneratedBy ECO_0000203 NP1103673.RA3I4i_OuK8_RCvwco1jv_GiC1jaemFi0hAMBHRoEM7RQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1103673.RA3I4i_OuK8_RCvwco1jv_GiC1jaemFi0hAMBHRoEM7RQ130_provenance.