Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1343123.RAyE0miI6gF4KpT7prptwoHivltDFDKo18fqhrH-PdnmE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1343123.RAyE0miI6gF4KpT7prptwoHivltDFDKo18fqhrH-PdnmE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1343123.RAyE0miI6gF4KpT7prptwoHivltDFDKo18fqhrH-PdnmE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1343123.RAyE0miI6gF4KpT7prptwoHivltDFDKo18fqhrH-PdnmE130_provenance.
- NP1343123.RAyE0miI6gF4KpT7prptwoHivltDFDKo18fqhrH-PdnmE130_assertion description "[A nonrandom translocation between chromosomes 3 and 21, t(3;21)(q26.2;q22) has been detected in patients with a myelodysplastic syndrome or acute myeloid leukemia after treatment (t-MDS/t-AML) for a primary malignant disease and in chronic myelogenous leukemia in blast crisis (CML-BC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1343123.RAyE0miI6gF4KpT7prptwoHivltDFDKo18fqhrH-PdnmE130_provenance.
- NP1343123.RAyE0miI6gF4KpT7prptwoHivltDFDKo18fqhrH-PdnmE130_assertion evidence source_evidence_literature NP1343123.RAyE0miI6gF4KpT7prptwoHivltDFDKo18fqhrH-PdnmE130_provenance.
- NP1343123.RAyE0miI6gF4KpT7prptwoHivltDFDKo18fqhrH-PdnmE130_assertion SIO_000772 8490181 NP1343123.RAyE0miI6gF4KpT7prptwoHivltDFDKo18fqhrH-PdnmE130_provenance.
- NP1343123.RAyE0miI6gF4KpT7prptwoHivltDFDKo18fqhrH-PdnmE130_assertion wasDerivedFrom befree-2016 NP1343123.RAyE0miI6gF4KpT7prptwoHivltDFDKo18fqhrH-PdnmE130_provenance.
- NP1343123.RAyE0miI6gF4KpT7prptwoHivltDFDKo18fqhrH-PdnmE130_assertion wasGeneratedBy ECO_0000203 NP1343123.RAyE0miI6gF4KpT7prptwoHivltDFDKo18fqhrH-PdnmE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1343123.RAyE0miI6gF4KpT7prptwoHivltDFDKo18fqhrH-PdnmE130_provenance.