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- source_evidence_literature type ECO_0000212 NP1170526.RAU-eBoN7Z-SWRqHleCy6AXfy4xys4UkmHNvMQfD1yizg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1170526.RAU-eBoN7Z-SWRqHleCy6AXfy4xys4UkmHNvMQfD1yizg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1170526.RAU-eBoN7Z-SWRqHleCy6AXfy4xys4UkmHNvMQfD1yizg130_provenance.
- NP1170526.RAU-eBoN7Z-SWRqHleCy6AXfy4xys4UkmHNvMQfD1yizg130_assertion description "[Sequence analysis of the tumor suppressor gene ASXL1, which is located in 20q and is commonly mutated in malignant myeloid diseases and occasionally in CLL/SLL specimens, revealed no mutations in our three patients with copy neutral LOH in 20q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1170526.RAU-eBoN7Z-SWRqHleCy6AXfy4xys4UkmHNvMQfD1yizg130_provenance.
- NP1170526.RAU-eBoN7Z-SWRqHleCy6AXfy4xys4UkmHNvMQfD1yizg130_assertion evidence source_evidence_literature NP1170526.RAU-eBoN7Z-SWRqHleCy6AXfy4xys4UkmHNvMQfD1yizg130_provenance.
- NP1170526.RAU-eBoN7Z-SWRqHleCy6AXfy4xys4UkmHNvMQfD1yizg130_assertion SIO_000772 24704113 NP1170526.RAU-eBoN7Z-SWRqHleCy6AXfy4xys4UkmHNvMQfD1yizg130_provenance.
- NP1170526.RAU-eBoN7Z-SWRqHleCy6AXfy4xys4UkmHNvMQfD1yizg130_assertion wasDerivedFrom befree-2016 NP1170526.RAU-eBoN7Z-SWRqHleCy6AXfy4xys4UkmHNvMQfD1yizg130_provenance.
- NP1170526.RAU-eBoN7Z-SWRqHleCy6AXfy4xys4UkmHNvMQfD1yizg130_assertion wasGeneratedBy ECO_0000203 NP1170526.RAU-eBoN7Z-SWRqHleCy6AXfy4xys4UkmHNvMQfD1yizg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1170526.RAU-eBoN7Z-SWRqHleCy6AXfy4xys4UkmHNvMQfD1yizg130_provenance.