Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP373529.RALpgyTWlNvHDXVf9lnMyIKOEl_zJtz7V6x7Zlr4GpyUo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP373529.RALpgyTWlNvHDXVf9lnMyIKOEl_zJtz7V6x7Zlr4GpyUo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP373529.RALpgyTWlNvHDXVf9lnMyIKOEl_zJtz7V6x7Zlr4GpyUo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP373529.RALpgyTWlNvHDXVf9lnMyIKOEl_zJtz7V6x7Zlr4GpyUo130_provenance.
- NP373529.RALpgyTWlNvHDXVf9lnMyIKOEl_zJtz7V6x7Zlr4GpyUo130_assertion description "[We show that UPD is a common chromosomal defect in myeloid malignancies, particularly in chronic myelomonocytic leukemia (CMML; 48%) and MDS/MPD-unclassifiable (38%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP373529.RALpgyTWlNvHDXVf9lnMyIKOEl_zJtz7V6x7Zlr4GpyUo130_provenance.
- NP373529.RALpgyTWlNvHDXVf9lnMyIKOEl_zJtz7V6x7Zlr4GpyUo130_assertion evidence source_evidence_literature NP373529.RALpgyTWlNvHDXVf9lnMyIKOEl_zJtz7V6x7Zlr4GpyUo130_provenance.
- NP373529.RALpgyTWlNvHDXVf9lnMyIKOEl_zJtz7V6x7Zlr4GpyUo130_assertion SIO_000772 19074904 NP373529.RALpgyTWlNvHDXVf9lnMyIKOEl_zJtz7V6x7Zlr4GpyUo130_provenance.
- NP373529.RALpgyTWlNvHDXVf9lnMyIKOEl_zJtz7V6x7Zlr4GpyUo130_assertion wasDerivedFrom befree-20140225 NP373529.RALpgyTWlNvHDXVf9lnMyIKOEl_zJtz7V6x7Zlr4GpyUo130_provenance.
- NP373529.RALpgyTWlNvHDXVf9lnMyIKOEl_zJtz7V6x7Zlr4GpyUo130_assertion wasGeneratedBy ECO_0000203 NP373529.RALpgyTWlNvHDXVf9lnMyIKOEl_zJtz7V6x7Zlr4GpyUo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP373529.RALpgyTWlNvHDXVf9lnMyIKOEl_zJtz7V6x7Zlr4GpyUo130_provenance.