Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP559538.RAImKIatYcn-psRdmtAqusnMWB5--pwVXcgBVhWv0bjKQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP559538.RAImKIatYcn-psRdmtAqusnMWB5--pwVXcgBVhWv0bjKQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP559538.RAImKIatYcn-psRdmtAqusnMWB5--pwVXcgBVhWv0bjKQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP559538.RAImKIatYcn-psRdmtAqusnMWB5--pwVXcgBVhWv0bjKQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP559538.RAImKIatYcn-psRdmtAqusnMWB5--pwVXcgBVhWv0bjKQ130_provenance.
- NP559538.RAImKIatYcn-psRdmtAqusnMWB5--pwVXcgBVhWv0bjKQ130_assertion wasGeneratedBy ECO_0000203 NP559538.RAImKIatYcn-psRdmtAqusnMWB5--pwVXcgBVhWv0bjKQ130_provenance.
- NP559538.RAImKIatYcn-psRdmtAqusnMWB5--pwVXcgBVhWv0bjKQ130_assertion wasDerivedFrom befree-2016 NP559538.RAImKIatYcn-psRdmtAqusnMWB5--pwVXcgBVhWv0bjKQ130_provenance.
- NP559538.RAImKIatYcn-psRdmtAqusnMWB5--pwVXcgBVhWv0bjKQ130_assertion SIO_000772 1683797 NP559538.RAImKIatYcn-psRdmtAqusnMWB5--pwVXcgBVhWv0bjKQ130_provenance.
- NP559538.RAImKIatYcn-psRdmtAqusnMWB5--pwVXcgBVhWv0bjKQ130_assertion evidence source_evidence_literature NP559538.RAImKIatYcn-psRdmtAqusnMWB5--pwVXcgBVhWv0bjKQ130_provenance.
- NP559538.RAImKIatYcn-psRdmtAqusnMWB5--pwVXcgBVhWv0bjKQ130_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." NP559538.RAImKIatYcn-psRdmtAqusnMWB5--pwVXcgBVhWv0bjKQ130_provenance.