Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP676353.RAGB0LdQQbBBdGL0pPnk7nWfPCIzKDOHl9l2KnWl9mVwI130_assertion> ?p ?o ?g. }
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- NP676353.RAGB0LdQQbBBdGL0pPnk7nWfPCIzKDOHl9l2KnWl9mVwI130_assertion type Assertion NP676353.RAGB0LdQQbBBdGL0pPnk7nWfPCIzKDOHl9l2KnWl9mVwI130_head.
- NP676353.RAGB0LdQQbBBdGL0pPnk7nWfPCIzKDOHl9l2KnWl9mVwI130_assertion description "[We conclude that, (1) p53 mutations are infrequent at diagnosis but tend to be associated with poor clinical outcome; (2) RAS and p21 mutations may not be involved in the pathogenesis of T-ALL; (3) not only frequent alterations of p16 and p15 genes but also methylation of p16 gene are involved in initiating the leukemogenesis of T-ALLs, and (4) these 5 genes are independently involved in T-ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676353.RAGB0LdQQbBBdGL0pPnk7nWfPCIzKDOHl9l2KnWl9mVwI130_provenance.
- NP676353.RAGB0LdQQbBBdGL0pPnk7nWfPCIzKDOHl9l2KnWl9mVwI130_assertion evidence source_evidence_literature NP676353.RAGB0LdQQbBBdGL0pPnk7nWfPCIzKDOHl9l2KnWl9mVwI130_provenance.
- NP676353.RAGB0LdQQbBBdGL0pPnk7nWfPCIzKDOHl9l2KnWl9mVwI130_assertion SIO_000772 10071127 NP676353.RAGB0LdQQbBBdGL0pPnk7nWfPCIzKDOHl9l2KnWl9mVwI130_provenance.
- NP676353.RAGB0LdQQbBBdGL0pPnk7nWfPCIzKDOHl9l2KnWl9mVwI130_assertion wasDerivedFrom befree-20140225 NP676353.RAGB0LdQQbBBdGL0pPnk7nWfPCIzKDOHl9l2KnWl9mVwI130_provenance.
- NP676353.RAGB0LdQQbBBdGL0pPnk7nWfPCIzKDOHl9l2KnWl9mVwI130_assertion wasGeneratedBy ECO_0000203 NP676353.RAGB0LdQQbBBdGL0pPnk7nWfPCIzKDOHl9l2KnWl9mVwI130_provenance.