Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP847704.RAHBZym5rAwNk4N-ynzKFpF3jlJczCDN5ubuy2lyV2aFc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP847704.RAHBZym5rAwNk4N-ynzKFpF3jlJczCDN5ubuy2lyV2aFc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP847704.RAHBZym5rAwNk4N-ynzKFpF3jlJczCDN5ubuy2lyV2aFc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP847704.RAHBZym5rAwNk4N-ynzKFpF3jlJczCDN5ubuy2lyV2aFc130_provenance.
- NP847704.RAHBZym5rAwNk4N-ynzKFpF3jlJczCDN5ubuy2lyV2aFc130_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." NP847704.RAHBZym5rAwNk4N-ynzKFpF3jlJczCDN5ubuy2lyV2aFc130_provenance.
- NP847704.RAHBZym5rAwNk4N-ynzKFpF3jlJczCDN5ubuy2lyV2aFc130_assertion evidence source_evidence_literature NP847704.RAHBZym5rAwNk4N-ynzKFpF3jlJczCDN5ubuy2lyV2aFc130_provenance.
- NP847704.RAHBZym5rAwNk4N-ynzKFpF3jlJczCDN5ubuy2lyV2aFc130_assertion SIO_000772 10071127 NP847704.RAHBZym5rAwNk4N-ynzKFpF3jlJczCDN5ubuy2lyV2aFc130_provenance.
- NP847704.RAHBZym5rAwNk4N-ynzKFpF3jlJczCDN5ubuy2lyV2aFc130_assertion wasDerivedFrom befree-20150227 NP847704.RAHBZym5rAwNk4N-ynzKFpF3jlJczCDN5ubuy2lyV2aFc130_provenance.
- NP847704.RAHBZym5rAwNk4N-ynzKFpF3jlJczCDN5ubuy2lyV2aFc130_assertion wasGeneratedBy ECO_0000203 NP847704.RAHBZym5rAwNk4N-ynzKFpF3jlJczCDN5ubuy2lyV2aFc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP847704.RAHBZym5rAwNk4N-ynzKFpF3jlJczCDN5ubuy2lyV2aFc130_provenance.