Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP504498.RAepTcTdGhPE7wnjL0Qor_Gc-SSP9Vi6QO3Hca2vAsZ5E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP504498.RAepTcTdGhPE7wnjL0Qor_Gc-SSP9Vi6QO3Hca2vAsZ5E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP504498.RAepTcTdGhPE7wnjL0Qor_Gc-SSP9Vi6QO3Hca2vAsZ5E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP504498.RAepTcTdGhPE7wnjL0Qor_Gc-SSP9Vi6QO3Hca2vAsZ5E130_provenance.
- NP504498.RAepTcTdGhPE7wnjL0Qor_Gc-SSP9Vi6QO3Hca2vAsZ5E130_assertion description "[This phenotype is induced by specific acute myeloid leukemia-associated translocations, such as t(15;17) and t(11;17), which involve an identical portion of the retinoic acid receptor alpha (RARalpha) and either the promyelocytic leukemia (PML) or promyelocytic zinc finger (PLZF) genes, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP504498.RAepTcTdGhPE7wnjL0Qor_Gc-SSP9Vi6QO3Hca2vAsZ5E130_provenance.
- NP504498.RAepTcTdGhPE7wnjL0Qor_Gc-SSP9Vi6QO3Hca2vAsZ5E130_assertion evidence source_evidence_literature NP504498.RAepTcTdGhPE7wnjL0Qor_Gc-SSP9Vi6QO3Hca2vAsZ5E130_provenance.
- NP504498.RAepTcTdGhPE7wnjL0Qor_Gc-SSP9Vi6QO3Hca2vAsZ5E130_assertion SIO_000772 16024608 NP504498.RAepTcTdGhPE7wnjL0Qor_Gc-SSP9Vi6QO3Hca2vAsZ5E130_provenance.
- NP504498.RAepTcTdGhPE7wnjL0Qor_Gc-SSP9Vi6QO3Hca2vAsZ5E130_assertion wasDerivedFrom befree-2016 NP504498.RAepTcTdGhPE7wnjL0Qor_Gc-SSP9Vi6QO3Hca2vAsZ5E130_provenance.
- NP504498.RAepTcTdGhPE7wnjL0Qor_Gc-SSP9Vi6QO3Hca2vAsZ5E130_assertion wasGeneratedBy ECO_0000203 NP504498.RAepTcTdGhPE7wnjL0Qor_Gc-SSP9Vi6QO3Hca2vAsZ5E130_provenance.
- befree-2016 importedOn "2016-02-19" NP504498.RAepTcTdGhPE7wnjL0Qor_Gc-SSP9Vi6QO3Hca2vAsZ5E130_provenance.