Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP878208.RA5NLm0Dsv17ocCT3OuO7ebU2SWl3sxp3l0h5aHEQkAEI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP878208.RA5NLm0Dsv17ocCT3OuO7ebU2SWl3sxp3l0h5aHEQkAEI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP878208.RA5NLm0Dsv17ocCT3OuO7ebU2SWl3sxp3l0h5aHEQkAEI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP878208.RA5NLm0Dsv17ocCT3OuO7ebU2SWl3sxp3l0h5aHEQkAEI130_provenance.
- befree-2016 importedOn "2016-02-19" NP878208.RA5NLm0Dsv17ocCT3OuO7ebU2SWl3sxp3l0h5aHEQkAEI130_provenance.
- NP878208.RA5NLm0Dsv17ocCT3OuO7ebU2SWl3sxp3l0h5aHEQkAEI130_assertion wasGeneratedBy ECO_0000203 NP878208.RA5NLm0Dsv17ocCT3OuO7ebU2SWl3sxp3l0h5aHEQkAEI130_provenance.
- NP878208.RA5NLm0Dsv17ocCT3OuO7ebU2SWl3sxp3l0h5aHEQkAEI130_assertion wasDerivedFrom befree-2016 NP878208.RA5NLm0Dsv17ocCT3OuO7ebU2SWl3sxp3l0h5aHEQkAEI130_provenance.
- NP878208.RA5NLm0Dsv17ocCT3OuO7ebU2SWl3sxp3l0h5aHEQkAEI130_assertion SIO_000772 21387358 NP878208.RA5NLm0Dsv17ocCT3OuO7ebU2SWl3sxp3l0h5aHEQkAEI130_provenance.
- NP878208.RA5NLm0Dsv17ocCT3OuO7ebU2SWl3sxp3l0h5aHEQkAEI130_assertion evidence source_evidence_literature NP878208.RA5NLm0Dsv17ocCT3OuO7ebU2SWl3sxp3l0h5aHEQkAEI130_provenance.
- NP878208.RA5NLm0Dsv17ocCT3OuO7ebU2SWl3sxp3l0h5aHEQkAEI130_assertion description "[Acute promyelocytic leukaemia (APL) with t(15;17);PML-RARα (n = 7/18; 39%) harboured the highest frequency of FLT3 mutations, followed by myelomonocytic (n = 4/18; 22%) and AML with t(8;21);RUNX1-RUNX1T1 (n = 2/21; 9%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP878208.RA5NLm0Dsv17ocCT3OuO7ebU2SWl3sxp3l0h5aHEQkAEI130_provenance.