Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP588459.RAy7K2Df04lbVxCoMO-2fOmyoOZc7jvAWdsNF5shlSECg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP588459.RAy7K2Df04lbVxCoMO-2fOmyoOZc7jvAWdsNF5shlSECg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP588459.RAy7K2Df04lbVxCoMO-2fOmyoOZc7jvAWdsNF5shlSECg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP588459.RAy7K2Df04lbVxCoMO-2fOmyoOZc7jvAWdsNF5shlSECg130_provenance.
- NP588459.RAy7K2Df04lbVxCoMO-2fOmyoOZc7jvAWdsNF5shlSECg130_assertion description "[The phenotypic overlap was explained by the involvement of the Ras pathway in both disorders, and, accordingly, clustering of the NF1 mutations in the GTPase-activating protein (GAP) domain of neurofibromin was observed in individuals with NFNS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588459.RAy7K2Df04lbVxCoMO-2fOmyoOZc7jvAWdsNF5shlSECg130_provenance.
- NP588459.RAy7K2Df04lbVxCoMO-2fOmyoOZc7jvAWdsNF5shlSECg130_assertion evidence source_evidence_literature NP588459.RAy7K2Df04lbVxCoMO-2fOmyoOZc7jvAWdsNF5shlSECg130_provenance.
- NP588459.RAy7K2Df04lbVxCoMO-2fOmyoOZc7jvAWdsNF5shlSECg130_assertion SIO_000772 19449407 NP588459.RAy7K2Df04lbVxCoMO-2fOmyoOZc7jvAWdsNF5shlSECg130_provenance.
- NP588459.RAy7K2Df04lbVxCoMO-2fOmyoOZc7jvAWdsNF5shlSECg130_assertion wasDerivedFrom befree-20150227 NP588459.RAy7K2Df04lbVxCoMO-2fOmyoOZc7jvAWdsNF5shlSECg130_provenance.
- NP588459.RAy7K2Df04lbVxCoMO-2fOmyoOZc7jvAWdsNF5shlSECg130_assertion wasGeneratedBy ECO_0000203 NP588459.RAy7K2Df04lbVxCoMO-2fOmyoOZc7jvAWdsNF5shlSECg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP588459.RAy7K2Df04lbVxCoMO-2fOmyoOZc7jvAWdsNF5shlSECg130_provenance.