Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP667025.RAYgiRk2vXvGvuwXLwparXM6jKflFyE9y0UjIybFd2MD8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP667025.RAYgiRk2vXvGvuwXLwparXM6jKflFyE9y0UjIybFd2MD8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP667025.RAYgiRk2vXvGvuwXLwparXM6jKflFyE9y0UjIybFd2MD8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP667025.RAYgiRk2vXvGvuwXLwparXM6jKflFyE9y0UjIybFd2MD8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP667025.RAYgiRk2vXvGvuwXLwparXM6jKflFyE9y0UjIybFd2MD8130_provenance.
- NP667025.RAYgiRk2vXvGvuwXLwparXM6jKflFyE9y0UjIybFd2MD8130_assertion wasGeneratedBy ECO_0000203 NP667025.RAYgiRk2vXvGvuwXLwparXM6jKflFyE9y0UjIybFd2MD8130_provenance.
- NP667025.RAYgiRk2vXvGvuwXLwparXM6jKflFyE9y0UjIybFd2MD8130_assertion wasDerivedFrom befree-20150227 NP667025.RAYgiRk2vXvGvuwXLwparXM6jKflFyE9y0UjIybFd2MD8130_provenance.
- NP667025.RAYgiRk2vXvGvuwXLwparXM6jKflFyE9y0UjIybFd2MD8130_assertion SIO_000772 1683797 NP667025.RAYgiRk2vXvGvuwXLwparXM6jKflFyE9y0UjIybFd2MD8130_provenance.
- NP667025.RAYgiRk2vXvGvuwXLwparXM6jKflFyE9y0UjIybFd2MD8130_assertion evidence source_evidence_literature NP667025.RAYgiRk2vXvGvuwXLwparXM6jKflFyE9y0UjIybFd2MD8130_provenance.
- NP667025.RAYgiRk2vXvGvuwXLwparXM6jKflFyE9y0UjIybFd2MD8130_assertion description "[Structural abnormalities of the Rb gene with absent protein expression were frequent in all types of human acute leukemia, but were particularly common (27% incidence) in M4 and M5 myeloid leukemia with monocytic differentiation and in Philadelphia chromosome (Ph1)-positive leukemia of lymphoid phenotype (11% to 29% incidence).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667025.RAYgiRk2vXvGvuwXLwparXM6jKflFyE9y0UjIybFd2MD8130_provenance.