Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP604757.RA00g1r10hGOs2aF4tct-DCuDix6t3Psqu_jTo0VtrarI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP604757.RA00g1r10hGOs2aF4tct-DCuDix6t3Psqu_jTo0VtrarI130_assertion type Assertion NP604757.RA00g1r10hGOs2aF4tct-DCuDix6t3Psqu_jTo0VtrarI130_head.
- NP604757.RA00g1r10hGOs2aF4tct-DCuDix6t3Psqu_jTo0VtrarI130_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." NP604757.RA00g1r10hGOs2aF4tct-DCuDix6t3Psqu_jTo0VtrarI130_provenance.
- NP604757.RA00g1r10hGOs2aF4tct-DCuDix6t3Psqu_jTo0VtrarI130_assertion evidence source_evidence_literature NP604757.RA00g1r10hGOs2aF4tct-DCuDix6t3Psqu_jTo0VtrarI130_provenance.
- NP604757.RA00g1r10hGOs2aF4tct-DCuDix6t3Psqu_jTo0VtrarI130_assertion SIO_000772 10602435 NP604757.RA00g1r10hGOs2aF4tct-DCuDix6t3Psqu_jTo0VtrarI130_provenance.
- NP604757.RA00g1r10hGOs2aF4tct-DCuDix6t3Psqu_jTo0VtrarI130_assertion wasDerivedFrom befree-20140225 NP604757.RA00g1r10hGOs2aF4tct-DCuDix6t3Psqu_jTo0VtrarI130_provenance.
- NP604757.RA00g1r10hGOs2aF4tct-DCuDix6t3Psqu_jTo0VtrarI130_assertion wasGeneratedBy ECO_0000203 NP604757.RA00g1r10hGOs2aF4tct-DCuDix6t3Psqu_jTo0VtrarI130_provenance.