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- source_evidence_literature type ECO_0000212 NP746647.RAir2rTu4v52oieohxese2_cfAzq0IXJmxEVLs6MshBKA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP746647.RAir2rTu4v52oieohxese2_cfAzq0IXJmxEVLs6MshBKA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP746647.RAir2rTu4v52oieohxese2_cfAzq0IXJmxEVLs6MshBKA130_provenance.
- NP746647.RAir2rTu4v52oieohxese2_cfAzq0IXJmxEVLs6MshBKA130_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." NP746647.RAir2rTu4v52oieohxese2_cfAzq0IXJmxEVLs6MshBKA130_provenance.
- NP746647.RAir2rTu4v52oieohxese2_cfAzq0IXJmxEVLs6MshBKA130_assertion evidence source_evidence_literature NP746647.RAir2rTu4v52oieohxese2_cfAzq0IXJmxEVLs6MshBKA130_provenance.
- NP746647.RAir2rTu4v52oieohxese2_cfAzq0IXJmxEVLs6MshBKA130_assertion SIO_000772 10071127 NP746647.RAir2rTu4v52oieohxese2_cfAzq0IXJmxEVLs6MshBKA130_provenance.
- NP746647.RAir2rTu4v52oieohxese2_cfAzq0IXJmxEVLs6MshBKA130_assertion wasDerivedFrom befree-20140225 NP746647.RAir2rTu4v52oieohxese2_cfAzq0IXJmxEVLs6MshBKA130_provenance.
- NP746647.RAir2rTu4v52oieohxese2_cfAzq0IXJmxEVLs6MshBKA130_assertion wasGeneratedBy ECO_0000203 NP746647.RAir2rTu4v52oieohxese2_cfAzq0IXJmxEVLs6MshBKA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP746647.RAir2rTu4v52oieohxese2_cfAzq0IXJmxEVLs6MshBKA130_provenance.