Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP227852.RAduGJnPkjSv1Clbdliy_e2waRl8_Dd1Zu5mL5L7M671c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP227852.RAduGJnPkjSv1Clbdliy_e2waRl8_Dd1Zu5mL5L7M671c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP227852.RAduGJnPkjSv1Clbdliy_e2waRl8_Dd1Zu5mL5L7M671c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP227852.RAduGJnPkjSv1Clbdliy_e2waRl8_Dd1Zu5mL5L7M671c130_provenance.
- NP227852.RAduGJnPkjSv1Clbdliy_e2waRl8_Dd1Zu5mL5L7M671c130_assertion wasGeneratedBy ECO_0000203 NP227852.RAduGJnPkjSv1Clbdliy_e2waRl8_Dd1Zu5mL5L7M671c130_provenance.
- NP227852.RAduGJnPkjSv1Clbdliy_e2waRl8_Dd1Zu5mL5L7M671c130_assertion wasDerivedFrom befree-20140225 NP227852.RAduGJnPkjSv1Clbdliy_e2waRl8_Dd1Zu5mL5L7M671c130_provenance.
- NP227852.RAduGJnPkjSv1Clbdliy_e2waRl8_Dd1Zu5mL5L7M671c130_assertion SIO_000772 8180390 NP227852.RAduGJnPkjSv1Clbdliy_e2waRl8_Dd1Zu5mL5L7M671c130_provenance.
- NP227852.RAduGJnPkjSv1Clbdliy_e2waRl8_Dd1Zu5mL5L7M671c130_assertion evidence source_evidence_literature NP227852.RAduGJnPkjSv1Clbdliy_e2waRl8_Dd1Zu5mL5L7M671c130_provenance.
- NP227852.RAduGJnPkjSv1Clbdliy_e2waRl8_Dd1Zu5mL5L7M671c130_assertion description "[Our results show that APL patients with cytogenetically normal chromosomes 15 and 17 may, nevertheless, have involvement of both PML and RARA genes defining a subgroup of APL, t(15;17)-negative/PML-RARA-positive which is analogous to Philadelphia chromosome-negative/BCR-ABL-positive CML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP227852.RAduGJnPkjSv1Clbdliy_e2waRl8_Dd1Zu5mL5L7M671c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP227852.RAduGJnPkjSv1Clbdliy_e2waRl8_Dd1Zu5mL5L7M671c130_provenance.