Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP212645.RAiEGJQFKeiJQaJF_PVU13AMdyUrGJy6phxC9nlooSjhw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP212645.RAiEGJQFKeiJQaJF_PVU13AMdyUrGJy6phxC9nlooSjhw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP212645.RAiEGJQFKeiJQaJF_PVU13AMdyUrGJy6phxC9nlooSjhw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP212645.RAiEGJQFKeiJQaJF_PVU13AMdyUrGJy6phxC9nlooSjhw130_provenance.
- NP212645.RAiEGJQFKeiJQaJF_PVU13AMdyUrGJy6phxC9nlooSjhw130_assertion description "[loss of one copy of PU.1 through deletion, plus down-regulation of the residual allele caused by PML-RARalpha expression, synergizes to expand myeloid progenitors susceptible to transformation, increasing the penetrance of acute promyelocytic leukemia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212645.RAiEGJQFKeiJQaJF_PVU13AMdyUrGJy6phxC9nlooSjhw130_provenance.
- NP212645.RAiEGJQFKeiJQaJF_PVU13AMdyUrGJy6phxC9nlooSjhw130_assertion evidence source_evidence_literature NP212645.RAiEGJQFKeiJQaJF_PVU13AMdyUrGJy6phxC9nlooSjhw130_provenance.
- NP212645.RAiEGJQFKeiJQaJF_PVU13AMdyUrGJy6phxC9nlooSjhw130_assertion SIO_000772 16113082 NP212645.RAiEGJQFKeiJQaJF_PVU13AMdyUrGJy6phxC9nlooSjhw130_provenance.
- NP212645.RAiEGJQFKeiJQaJF_PVU13AMdyUrGJy6phxC9nlooSjhw130_assertion wasDerivedFrom lhgdn-20090331 NP212645.RAiEGJQFKeiJQaJF_PVU13AMdyUrGJy6phxC9nlooSjhw130_provenance.
- NP212645.RAiEGJQFKeiJQaJF_PVU13AMdyUrGJy6phxC9nlooSjhw130_assertion wasGeneratedBy ECO_0000203 NP212645.RAiEGJQFKeiJQaJF_PVU13AMdyUrGJy6phxC9nlooSjhw130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP212645.RAiEGJQFKeiJQaJF_PVU13AMdyUrGJy6phxC9nlooSjhw130_provenance.