Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP327748.RAKtxt3RMhEV1DbsdQC-6IAZOI4KuVgcNGSm38Gej8wcQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP327748.RAKtxt3RMhEV1DbsdQC-6IAZOI4KuVgcNGSm38Gej8wcQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP327748.RAKtxt3RMhEV1DbsdQC-6IAZOI4KuVgcNGSm38Gej8wcQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP327748.RAKtxt3RMhEV1DbsdQC-6IAZOI4KuVgcNGSm38Gej8wcQ130_provenance.
- NP327748.RAKtxt3RMhEV1DbsdQC-6IAZOI4KuVgcNGSm38Gej8wcQ130_assertion description "[TEL/AML1 gene fusion that results from a cryptic t(12;21) is the most common genetic aberration in childhood B-lineage acute lymphoblastic leukemia (ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP327748.RAKtxt3RMhEV1DbsdQC-6IAZOI4KuVgcNGSm38Gej8wcQ130_provenance.
- NP327748.RAKtxt3RMhEV1DbsdQC-6IAZOI4KuVgcNGSm38Gej8wcQ130_assertion evidence source_evidence_literature NP327748.RAKtxt3RMhEV1DbsdQC-6IAZOI4KuVgcNGSm38Gej8wcQ130_provenance.
- NP327748.RAKtxt3RMhEV1DbsdQC-6IAZOI4KuVgcNGSm38Gej8wcQ130_assertion SIO_000772 11516105 NP327748.RAKtxt3RMhEV1DbsdQC-6IAZOI4KuVgcNGSm38Gej8wcQ130_provenance.
- NP327748.RAKtxt3RMhEV1DbsdQC-6IAZOI4KuVgcNGSm38Gej8wcQ130_assertion wasDerivedFrom befree-2016 NP327748.RAKtxt3RMhEV1DbsdQC-6IAZOI4KuVgcNGSm38Gej8wcQ130_provenance.
- NP327748.RAKtxt3RMhEV1DbsdQC-6IAZOI4KuVgcNGSm38Gej8wcQ130_assertion wasGeneratedBy ECO_0000203 NP327748.RAKtxt3RMhEV1DbsdQC-6IAZOI4KuVgcNGSm38Gej8wcQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP327748.RAKtxt3RMhEV1DbsdQC-6IAZOI4KuVgcNGSm38Gej8wcQ130_provenance.