Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP566863.RAsQ6GA7iKIQmqPY1OZN81Q-5RXE9JZ8F9ZcpkuTDY9LQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP566863.RAsQ6GA7iKIQmqPY1OZN81Q-5RXE9JZ8F9ZcpkuTDY9LQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP566863.RAsQ6GA7iKIQmqPY1OZN81Q-5RXE9JZ8F9ZcpkuTDY9LQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP566863.RAsQ6GA7iKIQmqPY1OZN81Q-5RXE9JZ8F9ZcpkuTDY9LQ130_provenance.
- NP566863.RAsQ6GA7iKIQmqPY1OZN81Q-5RXE9JZ8F9ZcpkuTDY9LQ130_assertion description "[By using probes specific for the c-mos and c-myc genes, we have analysed the genomic DNA from peripheral blood and bone marrow samples from 15 patients with various malignant myeloid diseases, including leukemia and myelodysplasia, and from one patient with non-Hodgkin's lymphoma, all of whom have trisomy for chromosome No.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP566863.RAsQ6GA7iKIQmqPY1OZN81Q-5RXE9JZ8F9ZcpkuTDY9LQ130_provenance.
- NP566863.RAsQ6GA7iKIQmqPY1OZN81Q-5RXE9JZ8F9ZcpkuTDY9LQ130_assertion evidence source_evidence_literature NP566863.RAsQ6GA7iKIQmqPY1OZN81Q-5RXE9JZ8F9ZcpkuTDY9LQ130_provenance.
- NP566863.RAsQ6GA7iKIQmqPY1OZN81Q-5RXE9JZ8F9ZcpkuTDY9LQ130_assertion SIO_000772 4079453 NP566863.RAsQ6GA7iKIQmqPY1OZN81Q-5RXE9JZ8F9ZcpkuTDY9LQ130_provenance.
- NP566863.RAsQ6GA7iKIQmqPY1OZN81Q-5RXE9JZ8F9ZcpkuTDY9LQ130_assertion wasDerivedFrom befree-20150227 NP566863.RAsQ6GA7iKIQmqPY1OZN81Q-5RXE9JZ8F9ZcpkuTDY9LQ130_provenance.
- NP566863.RAsQ6GA7iKIQmqPY1OZN81Q-5RXE9JZ8F9ZcpkuTDY9LQ130_assertion wasGeneratedBy ECO_0000203 NP566863.RAsQ6GA7iKIQmqPY1OZN81Q-5RXE9JZ8F9ZcpkuTDY9LQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP566863.RAsQ6GA7iKIQmqPY1OZN81Q-5RXE9JZ8F9ZcpkuTDY9LQ130_provenance.