Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1304539.RAtPNXVWjZoA9OovKJTNXsKUiN86q3EJ0LO4tmitc6LgI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1304539.RAtPNXVWjZoA9OovKJTNXsKUiN86q3EJ0LO4tmitc6LgI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1304539.RAtPNXVWjZoA9OovKJTNXsKUiN86q3EJ0LO4tmitc6LgI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1304539.RAtPNXVWjZoA9OovKJTNXsKUiN86q3EJ0LO4tmitc6LgI130_provenance.
- NP1304539.RAtPNXVWjZoA9OovKJTNXsKUiN86q3EJ0LO4tmitc6LgI130_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." NP1304539.RAtPNXVWjZoA9OovKJTNXsKUiN86q3EJ0LO4tmitc6LgI130_provenance.
- NP1304539.RAtPNXVWjZoA9OovKJTNXsKUiN86q3EJ0LO4tmitc6LgI130_assertion evidence source_evidence_literature NP1304539.RAtPNXVWjZoA9OovKJTNXsKUiN86q3EJ0LO4tmitc6LgI130_provenance.
- NP1304539.RAtPNXVWjZoA9OovKJTNXsKUiN86q3EJ0LO4tmitc6LgI130_assertion SIO_000772 4079453 NP1304539.RAtPNXVWjZoA9OovKJTNXsKUiN86q3EJ0LO4tmitc6LgI130_provenance.
- NP1304539.RAtPNXVWjZoA9OovKJTNXsKUiN86q3EJ0LO4tmitc6LgI130_assertion wasDerivedFrom befree-2016 NP1304539.RAtPNXVWjZoA9OovKJTNXsKUiN86q3EJ0LO4tmitc6LgI130_provenance.
- NP1304539.RAtPNXVWjZoA9OovKJTNXsKUiN86q3EJ0LO4tmitc6LgI130_assertion wasGeneratedBy ECO_0000203 NP1304539.RAtPNXVWjZoA9OovKJTNXsKUiN86q3EJ0LO4tmitc6LgI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1304539.RAtPNXVWjZoA9OovKJTNXsKUiN86q3EJ0LO4tmitc6LgI130_provenance.