Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP170876.RAOrRCZPPGRmNoFS_oNgM8BsiZAgRZXt1q-qpNnBgqy-U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP170876.RAOrRCZPPGRmNoFS_oNgM8BsiZAgRZXt1q-qpNnBgqy-U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP170876.RAOrRCZPPGRmNoFS_oNgM8BsiZAgRZXt1q-qpNnBgqy-U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP170876.RAOrRCZPPGRmNoFS_oNgM8BsiZAgRZXt1q-qpNnBgqy-U130_provenance.
- NP170876.RAOrRCZPPGRmNoFS_oNgM8BsiZAgRZXt1q-qpNnBgqy-U130_assertion description "[Molecular analysis of the t(15;17) translocation in 70 patients with acute promyelocytic leukemia (APL) confirmed that the breakpoints of chromosome 15 were located in two regions of the promyelocytic leukemia (PML) gene, mainly introns 3 and 6, whereas the breakpoints of chromosome 17 were consistently in intron 2 of the retinoic acid receptor alpha (RARA) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP170876.RAOrRCZPPGRmNoFS_oNgM8BsiZAgRZXt1q-qpNnBgqy-U130_provenance.
- NP170876.RAOrRCZPPGRmNoFS_oNgM8BsiZAgRZXt1q-qpNnBgqy-U130_assertion evidence source_evidence_literature NP170876.RAOrRCZPPGRmNoFS_oNgM8BsiZAgRZXt1q-qpNnBgqy-U130_provenance.
- NP170876.RAOrRCZPPGRmNoFS_oNgM8BsiZAgRZXt1q-qpNnBgqy-U130_assertion SIO_000772 7534109 NP170876.RAOrRCZPPGRmNoFS_oNgM8BsiZAgRZXt1q-qpNnBgqy-U130_provenance.
- NP170876.RAOrRCZPPGRmNoFS_oNgM8BsiZAgRZXt1q-qpNnBgqy-U130_assertion wasDerivedFrom befree-20140225 NP170876.RAOrRCZPPGRmNoFS_oNgM8BsiZAgRZXt1q-qpNnBgqy-U130_provenance.
- NP170876.RAOrRCZPPGRmNoFS_oNgM8BsiZAgRZXt1q-qpNnBgqy-U130_assertion wasGeneratedBy ECO_0000203 NP170876.RAOrRCZPPGRmNoFS_oNgM8BsiZAgRZXt1q-qpNnBgqy-U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP170876.RAOrRCZPPGRmNoFS_oNgM8BsiZAgRZXt1q-qpNnBgqy-U130_provenance.