Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1103672.RAfnai5u_3ijtuImA5UIQ9yX7FEH8inia3aUQ_U_6byhg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1103672.RAfnai5u_3ijtuImA5UIQ9yX7FEH8inia3aUQ_U_6byhg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1103672.RAfnai5u_3ijtuImA5UIQ9yX7FEH8inia3aUQ_U_6byhg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1103672.RAfnai5u_3ijtuImA5UIQ9yX7FEH8inia3aUQ_U_6byhg130_provenance.
- NP1103672.RAfnai5u_3ijtuImA5UIQ9yX7FEH8inia3aUQ_U_6byhg130_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." NP1103672.RAfnai5u_3ijtuImA5UIQ9yX7FEH8inia3aUQ_U_6byhg130_provenance.
- NP1103672.RAfnai5u_3ijtuImA5UIQ9yX7FEH8inia3aUQ_U_6byhg130_assertion evidence source_evidence_literature NP1103672.RAfnai5u_3ijtuImA5UIQ9yX7FEH8inia3aUQ_U_6byhg130_provenance.
- NP1103672.RAfnai5u_3ijtuImA5UIQ9yX7FEH8inia3aUQ_U_6byhg130_assertion SIO_000772 23958953 NP1103672.RAfnai5u_3ijtuImA5UIQ9yX7FEH8inia3aUQ_U_6byhg130_provenance.
- NP1103672.RAfnai5u_3ijtuImA5UIQ9yX7FEH8inia3aUQ_U_6byhg130_assertion wasDerivedFrom befree-2016 NP1103672.RAfnai5u_3ijtuImA5UIQ9yX7FEH8inia3aUQ_U_6byhg130_provenance.
- NP1103672.RAfnai5u_3ijtuImA5UIQ9yX7FEH8inia3aUQ_U_6byhg130_assertion wasGeneratedBy ECO_0000203 NP1103672.RAfnai5u_3ijtuImA5UIQ9yX7FEH8inia3aUQ_U_6byhg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1103672.RAfnai5u_3ijtuImA5UIQ9yX7FEH8inia3aUQ_U_6byhg130_provenance.