Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP585073.RA0kMt9hwLIyBGmudN-mesiYwhN7DDmKAD_z_N_qF2XiE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP585073.RA0kMt9hwLIyBGmudN-mesiYwhN7DDmKAD_z_N_qF2XiE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP585073.RA0kMt9hwLIyBGmudN-mesiYwhN7DDmKAD_z_N_qF2XiE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP585073.RA0kMt9hwLIyBGmudN-mesiYwhN7DDmKAD_z_N_qF2XiE130_provenance.
- befree-2016 importedOn "2016-02-19" NP585073.RA0kMt9hwLIyBGmudN-mesiYwhN7DDmKAD_z_N_qF2XiE130_provenance.
- NP585073.RA0kMt9hwLIyBGmudN-mesiYwhN7DDmKAD_z_N_qF2XiE130_assertion wasGeneratedBy ECO_0000203 NP585073.RA0kMt9hwLIyBGmudN-mesiYwhN7DDmKAD_z_N_qF2XiE130_provenance.
- NP585073.RA0kMt9hwLIyBGmudN-mesiYwhN7DDmKAD_z_N_qF2XiE130_assertion wasDerivedFrom befree-2016 NP585073.RA0kMt9hwLIyBGmudN-mesiYwhN7DDmKAD_z_N_qF2XiE130_provenance.
- NP585073.RA0kMt9hwLIyBGmudN-mesiYwhN7DDmKAD_z_N_qF2XiE130_assertion SIO_000772 17178874 NP585073.RA0kMt9hwLIyBGmudN-mesiYwhN7DDmKAD_z_N_qF2XiE130_provenance.
- NP585073.RA0kMt9hwLIyBGmudN-mesiYwhN7DDmKAD_z_N_qF2XiE130_assertion evidence source_evidence_literature NP585073.RA0kMt9hwLIyBGmudN-mesiYwhN7DDmKAD_z_N_qF2XiE130_provenance.
- NP585073.RA0kMt9hwLIyBGmudN-mesiYwhN7DDmKAD_z_N_qF2XiE130_assertion description "[The t(7;11)(p15;p15) translocation, observed in acute myelogenous leukemia and myelodysplastic syndrome, generates a chimeric gene where the 5' portion of the sequence encoding the human nucleoporin NUP98 protein is fused to the 3' region of HOXA9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP585073.RA0kMt9hwLIyBGmudN-mesiYwhN7DDmKAD_z_N_qF2XiE130_provenance.