Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP655680.RAeP4eCSmP-PhypCcXy_-yLf2U1A2-ZLl36CsvsMWXRIw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP655680.RAeP4eCSmP-PhypCcXy_-yLf2U1A2-ZLl36CsvsMWXRIw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP655680.RAeP4eCSmP-PhypCcXy_-yLf2U1A2-ZLl36CsvsMWXRIw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP655680.RAeP4eCSmP-PhypCcXy_-yLf2U1A2-ZLl36CsvsMWXRIw130_provenance.
- NP655680.RAeP4eCSmP-PhypCcXy_-yLf2U1A2-ZLl36CsvsMWXRIw130_assertion description "[To our knowledge, this is the first case reported with subtelomeric t(5;9)(q35.3;q34.3) and the deletion of the RB1 gene in a patient with AML-M0.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP655680.RAeP4eCSmP-PhypCcXy_-yLf2U1A2-ZLl36CsvsMWXRIw130_provenance.
- NP655680.RAeP4eCSmP-PhypCcXy_-yLf2U1A2-ZLl36CsvsMWXRIw130_assertion evidence source_evidence_literature NP655680.RAeP4eCSmP-PhypCcXy_-yLf2U1A2-ZLl36CsvsMWXRIw130_provenance.
- NP655680.RAeP4eCSmP-PhypCcXy_-yLf2U1A2-ZLl36CsvsMWXRIw130_assertion SIO_000772 18262051 NP655680.RAeP4eCSmP-PhypCcXy_-yLf2U1A2-ZLl36CsvsMWXRIw130_provenance.
- NP655680.RAeP4eCSmP-PhypCcXy_-yLf2U1A2-ZLl36CsvsMWXRIw130_assertion wasDerivedFrom befree-20140225 NP655680.RAeP4eCSmP-PhypCcXy_-yLf2U1A2-ZLl36CsvsMWXRIw130_provenance.
- NP655680.RAeP4eCSmP-PhypCcXy_-yLf2U1A2-ZLl36CsvsMWXRIw130_assertion wasGeneratedBy ECO_0000203 NP655680.RAeP4eCSmP-PhypCcXy_-yLf2U1A2-ZLl36CsvsMWXRIw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP655680.RAeP4eCSmP-PhypCcXy_-yLf2U1A2-ZLl36CsvsMWXRIw130_provenance.