Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP322089.RAbGdQS8cF7yoMeruA995eUAPrV_6vYWLqcMz5ARD5JSY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP322089.RAbGdQS8cF7yoMeruA995eUAPrV_6vYWLqcMz5ARD5JSY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP322089.RAbGdQS8cF7yoMeruA995eUAPrV_6vYWLqcMz5ARD5JSY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP322089.RAbGdQS8cF7yoMeruA995eUAPrV_6vYWLqcMz5ARD5JSY130_provenance.
- NP322089.RAbGdQS8cF7yoMeruA995eUAPrV_6vYWLqcMz5ARD5JSY130_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." NP322089.RAbGdQS8cF7yoMeruA995eUAPrV_6vYWLqcMz5ARD5JSY130_provenance.
- NP322089.RAbGdQS8cF7yoMeruA995eUAPrV_6vYWLqcMz5ARD5JSY130_assertion evidence source_evidence_literature NP322089.RAbGdQS8cF7yoMeruA995eUAPrV_6vYWLqcMz5ARD5JSY130_provenance.
- NP322089.RAbGdQS8cF7yoMeruA995eUAPrV_6vYWLqcMz5ARD5JSY130_assertion SIO_000772 15958502 NP322089.RAbGdQS8cF7yoMeruA995eUAPrV_6vYWLqcMz5ARD5JSY130_provenance.
- NP322089.RAbGdQS8cF7yoMeruA995eUAPrV_6vYWLqcMz5ARD5JSY130_assertion wasDerivedFrom befree-20140225 NP322089.RAbGdQS8cF7yoMeruA995eUAPrV_6vYWLqcMz5ARD5JSY130_provenance.
- NP322089.RAbGdQS8cF7yoMeruA995eUAPrV_6vYWLqcMz5ARD5JSY130_assertion wasGeneratedBy ECO_0000203 NP322089.RAbGdQS8cF7yoMeruA995eUAPrV_6vYWLqcMz5ARD5JSY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP322089.RAbGdQS8cF7yoMeruA995eUAPrV_6vYWLqcMz5ARD5JSY130_provenance.