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- source_evidence_literature type ECO_0000212 NP858229.RAnPydxRA4W_BXgetGM7StF9FsbVmU7FtVLnQhVeFd8fA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP858229.RAnPydxRA4W_BXgetGM7StF9FsbVmU7FtVLnQhVeFd8fA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP858229.RAnPydxRA4W_BXgetGM7StF9FsbVmU7FtVLnQhVeFd8fA130_provenance.
- NP858229.RAnPydxRA4W_BXgetGM7StF9FsbVmU7FtVLnQhVeFd8fA130_assertion description "[Since it has been proposed that especially neoplasias lacking p53 alterations might show a loss of heterozygosity at 1p35-1p36, we studied the frequency of p53 and p73 deletions in bone marrow mononuclear cells of 68 patients with MM, two patients with monoclonal gammopathy of undetermined significance and four patients with plasma cell leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP858229.RAnPydxRA4W_BXgetGM7StF9FsbVmU7FtVLnQhVeFd8fA130_provenance.
- NP858229.RAnPydxRA4W_BXgetGM7StF9FsbVmU7FtVLnQhVeFd8fA130_assertion evidence source_evidence_literature NP858229.RAnPydxRA4W_BXgetGM7StF9FsbVmU7FtVLnQhVeFd8fA130_provenance.
- NP858229.RAnPydxRA4W_BXgetGM7StF9FsbVmU7FtVLnQhVeFd8fA130_assertion SIO_000772 10602435 NP858229.RAnPydxRA4W_BXgetGM7StF9FsbVmU7FtVLnQhVeFd8fA130_provenance.
- NP858229.RAnPydxRA4W_BXgetGM7StF9FsbVmU7FtVLnQhVeFd8fA130_assertion wasDerivedFrom befree-20140225 NP858229.RAnPydxRA4W_BXgetGM7StF9FsbVmU7FtVLnQhVeFd8fA130_provenance.
- NP858229.RAnPydxRA4W_BXgetGM7StF9FsbVmU7FtVLnQhVeFd8fA130_assertion wasGeneratedBy ECO_0000203 NP858229.RAnPydxRA4W_BXgetGM7StF9FsbVmU7FtVLnQhVeFd8fA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP858229.RAnPydxRA4W_BXgetGM7StF9FsbVmU7FtVLnQhVeFd8fA130_provenance.