Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP412148.RAqax_LYnxDV11l28Vkz34hEILwLuqxOUChu_HDp-vRiM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP412148.RAqax_LYnxDV11l28Vkz34hEILwLuqxOUChu_HDp-vRiM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP412148.RAqax_LYnxDV11l28Vkz34hEILwLuqxOUChu_HDp-vRiM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP412148.RAqax_LYnxDV11l28Vkz34hEILwLuqxOUChu_HDp-vRiM130_provenance.
- NP412148.RAqax_LYnxDV11l28Vkz34hEILwLuqxOUChu_HDp-vRiM130_assertion description "[The molecular pathways involved in the aetiology of these syndromes have recently been more clearly defined and several major cellular signalling pathways are probably involved: the protein kinase A (PKA) pathway in Carney complex (CNC), the Ras/Erk MAP kinase pathway in LEOPARD/Noonan syndromes, and the mammalian target of rapamycin pathway (mTOR) in Peutz-Jeghers syndrome and the diseases caused by PTEN mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412148.RAqax_LYnxDV11l28Vkz34hEILwLuqxOUChu_HDp-vRiM130_provenance.
- NP412148.RAqax_LYnxDV11l28Vkz34hEILwLuqxOUChu_HDp-vRiM130_assertion evidence source_evidence_literature NP412148.RAqax_LYnxDV11l28Vkz34hEILwLuqxOUChu_HDp-vRiM130_provenance.
- NP412148.RAqax_LYnxDV11l28Vkz34hEILwLuqxOUChu_HDp-vRiM130_assertion SIO_000772 15958502 NP412148.RAqax_LYnxDV11l28Vkz34hEILwLuqxOUChu_HDp-vRiM130_provenance.
- NP412148.RAqax_LYnxDV11l28Vkz34hEILwLuqxOUChu_HDp-vRiM130_assertion wasDerivedFrom befree-20150227 NP412148.RAqax_LYnxDV11l28Vkz34hEILwLuqxOUChu_HDp-vRiM130_provenance.
- NP412148.RAqax_LYnxDV11l28Vkz34hEILwLuqxOUChu_HDp-vRiM130_assertion wasGeneratedBy ECO_0000203 NP412148.RAqax_LYnxDV11l28Vkz34hEILwLuqxOUChu_HDp-vRiM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP412148.RAqax_LYnxDV11l28Vkz34hEILwLuqxOUChu_HDp-vRiM130_provenance.