Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1393931.RAmBTuPhCSfHmc82Z1ED7SdzclTSpWHmR2YzscH_y-dXY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1393931.RAmBTuPhCSfHmc82Z1ED7SdzclTSpWHmR2YzscH_y-dXY130_assertion type Assertion NP1393931.RAmBTuPhCSfHmc82Z1ED7SdzclTSpWHmR2YzscH_y-dXY130_head.
- NP1393931.RAmBTuPhCSfHmc82Z1ED7SdzclTSpWHmR2YzscH_y-dXY130_assertion description "[In contrast with the molecular findings observed in chronic lymphocytic leukemia, our results indicate that trisomy 12 is an uncommon chromosomal aberration in SLVLs, and microdeletion of 13q14 at the RB1 locus but not D13S25 is a frequent and specific genetic event in this disease, suggesting that allelic loss of the RB1 gene may play a role in the pathogenesis of SLVL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1393931.RAmBTuPhCSfHmc82Z1ED7SdzclTSpWHmR2YzscH_y-dXY130_provenance.
- NP1393931.RAmBTuPhCSfHmc82Z1ED7SdzclTSpWHmR2YzscH_y-dXY130_assertion evidence source_evidence_literature NP1393931.RAmBTuPhCSfHmc82Z1ED7SdzclTSpWHmR2YzscH_y-dXY130_provenance.
- NP1393931.RAmBTuPhCSfHmc82Z1ED7SdzclTSpWHmR2YzscH_y-dXY130_assertion SIO_000772 9563492 NP1393931.RAmBTuPhCSfHmc82Z1ED7SdzclTSpWHmR2YzscH_y-dXY130_provenance.
- NP1393931.RAmBTuPhCSfHmc82Z1ED7SdzclTSpWHmR2YzscH_y-dXY130_assertion wasDerivedFrom befree-2016 NP1393931.RAmBTuPhCSfHmc82Z1ED7SdzclTSpWHmR2YzscH_y-dXY130_provenance.
- NP1393931.RAmBTuPhCSfHmc82Z1ED7SdzclTSpWHmR2YzscH_y-dXY130_assertion wasGeneratedBy ECO_0000203 NP1393931.RAmBTuPhCSfHmc82Z1ED7SdzclTSpWHmR2YzscH_y-dXY130_provenance.