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- NP177268.RAON_Pk4QtKXI_A1bKwyI4BkKokQe4tJ5BXg2Zsrv47TY130_assertion type Assertion NP177268.RAON_Pk4QtKXI_A1bKwyI4BkKokQe4tJ5BXg2Zsrv47TY130_head.
- NP177268.RAON_Pk4QtKXI_A1bKwyI4BkKokQe4tJ5BXg2Zsrv47TY130_assertion description "[Cowden disease (CD) is a genetically heterogeneous inherited cancer syndrome that arises predominantly from germline phosphatase and tensin homologue deleted on chromosome 10 (PTEN) mutation and increased phosphoinositide 3-kinase/mammalian target of rapamycin (PI3K/mTOR) signalling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177268.RAON_Pk4QtKXI_A1bKwyI4BkKokQe4tJ5BXg2Zsrv47TY130_provenance.
- NP177268.RAON_Pk4QtKXI_A1bKwyI4BkKokQe4tJ5BXg2Zsrv47TY130_assertion evidence source_evidence_literature NP177268.RAON_Pk4QtKXI_A1bKwyI4BkKokQe4tJ5BXg2Zsrv47TY130_provenance.
- NP177268.RAON_Pk4QtKXI_A1bKwyI4BkKokQe4tJ5BXg2Zsrv47TY130_assertion SIO_000772 21361912 NP177268.RAON_Pk4QtKXI_A1bKwyI4BkKokQe4tJ5BXg2Zsrv47TY130_provenance.
- NP177268.RAON_Pk4QtKXI_A1bKwyI4BkKokQe4tJ5BXg2Zsrv47TY130_assertion wasDerivedFrom befree-20140225 NP177268.RAON_Pk4QtKXI_A1bKwyI4BkKokQe4tJ5BXg2Zsrv47TY130_provenance.
- NP177268.RAON_Pk4QtKXI_A1bKwyI4BkKokQe4tJ5BXg2Zsrv47TY130_assertion wasGeneratedBy ECO_0000203 NP177268.RAON_Pk4QtKXI_A1bKwyI4BkKokQe4tJ5BXg2Zsrv47TY130_provenance.