Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP873288.RAYIGDn5Dpr953GdJQJOauSFn-PWJ4RSEf7VfNolZr8x4130_assertion> ?p ?o ?g. }
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- NP873288.RAYIGDn5Dpr953GdJQJOauSFn-PWJ4RSEf7VfNolZr8x4130_assertion type Assertion NP873288.RAYIGDn5Dpr953GdJQJOauSFn-PWJ4RSEf7VfNolZr8x4130_head.
- NP873288.RAYIGDn5Dpr953GdJQJOauSFn-PWJ4RSEf7VfNolZr8x4130_assertion description "[In the University of Chicago's series of 386 patients with t-MDS/t-AML, 79 (20%) patients had abnormalities of chromosome 5, 95 (25%) patients had abnormalities of chromosome 7, and 85 (22%) patients had abnormalities of both chromosomes 5 and 7. t-MDS/t-AML with a -5/del(5q) is associated with a complex karyotype, characterized by trisomy 8, as well as loss of 12p, 13q, 16q22, 17p (TP53 locus), chromosome 18, and 20q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873288.RAYIGDn5Dpr953GdJQJOauSFn-PWJ4RSEf7VfNolZr8x4130_provenance.
- NP873288.RAYIGDn5Dpr953GdJQJOauSFn-PWJ4RSEf7VfNolZr8x4130_assertion evidence source_evidence_literature NP873288.RAYIGDn5Dpr953GdJQJOauSFn-PWJ4RSEf7VfNolZr8x4130_provenance.
- NP873288.RAYIGDn5Dpr953GdJQJOauSFn-PWJ4RSEf7VfNolZr8x4130_assertion SIO_000772 19958752 NP873288.RAYIGDn5Dpr953GdJQJOauSFn-PWJ4RSEf7VfNolZr8x4130_provenance.
- NP873288.RAYIGDn5Dpr953GdJQJOauSFn-PWJ4RSEf7VfNolZr8x4130_assertion wasDerivedFrom befree-20150227 NP873288.RAYIGDn5Dpr953GdJQJOauSFn-PWJ4RSEf7VfNolZr8x4130_provenance.
- NP873288.RAYIGDn5Dpr953GdJQJOauSFn-PWJ4RSEf7VfNolZr8x4130_assertion wasGeneratedBy ECO_0000203 NP873288.RAYIGDn5Dpr953GdJQJOauSFn-PWJ4RSEf7VfNolZr8x4130_provenance.