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- source_evidence_literature type ECO_0000212 NP625044.RAGlWkZBRw1AnsJFuQFF_5pS5b3-j7KEnmyNERIhmWa5I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP625044.RAGlWkZBRw1AnsJFuQFF_5pS5b3-j7KEnmyNERIhmWa5I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP625044.RAGlWkZBRw1AnsJFuQFF_5pS5b3-j7KEnmyNERIhmWa5I130_provenance.
- NP625044.RAGlWkZBRw1AnsJFuQFF_5pS5b3-j7KEnmyNERIhmWa5I130_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." NP625044.RAGlWkZBRw1AnsJFuQFF_5pS5b3-j7KEnmyNERIhmWa5I130_provenance.
- NP625044.RAGlWkZBRw1AnsJFuQFF_5pS5b3-j7KEnmyNERIhmWa5I130_assertion evidence source_evidence_literature NP625044.RAGlWkZBRw1AnsJFuQFF_5pS5b3-j7KEnmyNERIhmWa5I130_provenance.
- NP625044.RAGlWkZBRw1AnsJFuQFF_5pS5b3-j7KEnmyNERIhmWa5I130_assertion SIO_000772 21361912 NP625044.RAGlWkZBRw1AnsJFuQFF_5pS5b3-j7KEnmyNERIhmWa5I130_provenance.
- NP625044.RAGlWkZBRw1AnsJFuQFF_5pS5b3-j7KEnmyNERIhmWa5I130_assertion wasDerivedFrom befree-20150227 NP625044.RAGlWkZBRw1AnsJFuQFF_5pS5b3-j7KEnmyNERIhmWa5I130_provenance.
- NP625044.RAGlWkZBRw1AnsJFuQFF_5pS5b3-j7KEnmyNERIhmWa5I130_assertion wasGeneratedBy ECO_0000203 NP625044.RAGlWkZBRw1AnsJFuQFF_5pS5b3-j7KEnmyNERIhmWa5I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP625044.RAGlWkZBRw1AnsJFuQFF_5pS5b3-j7KEnmyNERIhmWa5I130_provenance.