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- NP271351.RANUPBDCzbZIMOQj83lY8iTWSjw4_3hTEx1hXX66hHsFY130_assertion type Assertion NP271351.RANUPBDCzbZIMOQj83lY8iTWSjw4_3hTEx1hXX66hHsFY130_head.
- NP271351.RANUPBDCzbZIMOQj83lY8iTWSjw4_3hTEx1hXX66hHsFY130_assertion description "[Allelic loss of 13q14 was observed in 63.2% patients, most of them showing D13S319 and D13S25 deletion; 11% of patients showed TP53 monosomy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP271351.RANUPBDCzbZIMOQj83lY8iTWSjw4_3hTEx1hXX66hHsFY130_provenance.
- NP271351.RANUPBDCzbZIMOQj83lY8iTWSjw4_3hTEx1hXX66hHsFY130_assertion evidence source_evidence_literature NP271351.RANUPBDCzbZIMOQj83lY8iTWSjw4_3hTEx1hXX66hHsFY130_provenance.
- NP271351.RANUPBDCzbZIMOQj83lY8iTWSjw4_3hTEx1hXX66hHsFY130_assertion SIO_000772 14553950 NP271351.RANUPBDCzbZIMOQj83lY8iTWSjw4_3hTEx1hXX66hHsFY130_provenance.
- NP271351.RANUPBDCzbZIMOQj83lY8iTWSjw4_3hTEx1hXX66hHsFY130_assertion wasDerivedFrom befree-20140225 NP271351.RANUPBDCzbZIMOQj83lY8iTWSjw4_3hTEx1hXX66hHsFY130_provenance.
- NP271351.RANUPBDCzbZIMOQj83lY8iTWSjw4_3hTEx1hXX66hHsFY130_assertion wasGeneratedBy ECO_0000203 NP271351.RANUPBDCzbZIMOQj83lY8iTWSjw4_3hTEx1hXX66hHsFY130_provenance.