Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP465406.RA5eV2oadfJfntScYdMY8Bxr_PItc-PXWbyO21y6J-Vd0130_assertion> ?p ?o ?g. }
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- NP465406.RA5eV2oadfJfntScYdMY8Bxr_PItc-PXWbyO21y6J-Vd0130_assertion type Assertion NP465406.RA5eV2oadfJfntScYdMY8Bxr_PItc-PXWbyO21y6J-Vd0130_head.
- NP465406.RA5eV2oadfJfntScYdMY8Bxr_PItc-PXWbyO21y6J-Vd0130_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." NP465406.RA5eV2oadfJfntScYdMY8Bxr_PItc-PXWbyO21y6J-Vd0130_provenance.
- NP465406.RA5eV2oadfJfntScYdMY8Bxr_PItc-PXWbyO21y6J-Vd0130_assertion evidence source_evidence_literature NP465406.RA5eV2oadfJfntScYdMY8Bxr_PItc-PXWbyO21y6J-Vd0130_provenance.
- NP465406.RA5eV2oadfJfntScYdMY8Bxr_PItc-PXWbyO21y6J-Vd0130_assertion SIO_000772 9563492 NP465406.RA5eV2oadfJfntScYdMY8Bxr_PItc-PXWbyO21y6J-Vd0130_provenance.
- NP465406.RA5eV2oadfJfntScYdMY8Bxr_PItc-PXWbyO21y6J-Vd0130_assertion wasDerivedFrom befree-20140225 NP465406.RA5eV2oadfJfntScYdMY8Bxr_PItc-PXWbyO21y6J-Vd0130_provenance.
- NP465406.RA5eV2oadfJfntScYdMY8Bxr_PItc-PXWbyO21y6J-Vd0130_assertion wasGeneratedBy ECO_0000203 NP465406.RA5eV2oadfJfntScYdMY8Bxr_PItc-PXWbyO21y6J-Vd0130_provenance.