Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP859500.RAu-8oO7eGc--r2VnsFoNWUSIRGHKyNgXPs0LPuPLQhUg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP859500.RAu-8oO7eGc--r2VnsFoNWUSIRGHKyNgXPs0LPuPLQhUg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP859500.RAu-8oO7eGc--r2VnsFoNWUSIRGHKyNgXPs0LPuPLQhUg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP859500.RAu-8oO7eGc--r2VnsFoNWUSIRGHKyNgXPs0LPuPLQhUg130_provenance.
- NP859500.RAu-8oO7eGc--r2VnsFoNWUSIRGHKyNgXPs0LPuPLQhUg130_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." NP859500.RAu-8oO7eGc--r2VnsFoNWUSIRGHKyNgXPs0LPuPLQhUg130_provenance.
- NP859500.RAu-8oO7eGc--r2VnsFoNWUSIRGHKyNgXPs0LPuPLQhUg130_assertion evidence source_evidence_literature NP859500.RAu-8oO7eGc--r2VnsFoNWUSIRGHKyNgXPs0LPuPLQhUg130_provenance.
- NP859500.RAu-8oO7eGc--r2VnsFoNWUSIRGHKyNgXPs0LPuPLQhUg130_assertion SIO_000772 10602435 NP859500.RAu-8oO7eGc--r2VnsFoNWUSIRGHKyNgXPs0LPuPLQhUg130_provenance.
- NP859500.RAu-8oO7eGc--r2VnsFoNWUSIRGHKyNgXPs0LPuPLQhUg130_assertion wasDerivedFrom befree-20140225 NP859500.RAu-8oO7eGc--r2VnsFoNWUSIRGHKyNgXPs0LPuPLQhUg130_provenance.
- NP859500.RAu-8oO7eGc--r2VnsFoNWUSIRGHKyNgXPs0LPuPLQhUg130_assertion wasGeneratedBy ECO_0000203 NP859500.RAu-8oO7eGc--r2VnsFoNWUSIRGHKyNgXPs0LPuPLQhUg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP859500.RAu-8oO7eGc--r2VnsFoNWUSIRGHKyNgXPs0LPuPLQhUg130_provenance.