Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP551491.RAdzrzjo02g99rUFoL0e1I8YDC-KxlkGLMKIBY2QpgAu4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP551491.RAdzrzjo02g99rUFoL0e1I8YDC-KxlkGLMKIBY2QpgAu4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP551491.RAdzrzjo02g99rUFoL0e1I8YDC-KxlkGLMKIBY2QpgAu4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP551491.RAdzrzjo02g99rUFoL0e1I8YDC-KxlkGLMKIBY2QpgAu4130_provenance.
- NP551491.RAdzrzjo02g99rUFoL0e1I8YDC-KxlkGLMKIBY2QpgAu4130_assertion description "[This loss of one CSF1R allele, together with loss in some cells of the remaining allele on the homologous chromosome 5, in patients with myelodysplasia indicates that this is a region of critical gene loss on 5q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP551491.RAdzrzjo02g99rUFoL0e1I8YDC-KxlkGLMKIBY2QpgAu4130_provenance.
- NP551491.RAdzrzjo02g99rUFoL0e1I8YDC-KxlkGLMKIBY2QpgAu4130_assertion evidence source_evidence_literature NP551491.RAdzrzjo02g99rUFoL0e1I8YDC-KxlkGLMKIBY2QpgAu4130_provenance.
- NP551491.RAdzrzjo02g99rUFoL0e1I8YDC-KxlkGLMKIBY2QpgAu4130_assertion SIO_000772 1829836 NP551491.RAdzrzjo02g99rUFoL0e1I8YDC-KxlkGLMKIBY2QpgAu4130_provenance.
- NP551491.RAdzrzjo02g99rUFoL0e1I8YDC-KxlkGLMKIBY2QpgAu4130_assertion wasDerivedFrom befree-20140225 NP551491.RAdzrzjo02g99rUFoL0e1I8YDC-KxlkGLMKIBY2QpgAu4130_provenance.
- NP551491.RAdzrzjo02g99rUFoL0e1I8YDC-KxlkGLMKIBY2QpgAu4130_assertion wasGeneratedBy ECO_0000203 NP551491.RAdzrzjo02g99rUFoL0e1I8YDC-KxlkGLMKIBY2QpgAu4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP551491.RAdzrzjo02g99rUFoL0e1I8YDC-KxlkGLMKIBY2QpgAu4130_provenance.