Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP990994.RAabS4VfBL4vZEjOs-RJLVrIWoLfQTKssZDoTMN3P19jc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP990994.RAabS4VfBL4vZEjOs-RJLVrIWoLfQTKssZDoTMN3P19jc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP990994.RAabS4VfBL4vZEjOs-RJLVrIWoLfQTKssZDoTMN3P19jc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP990994.RAabS4VfBL4vZEjOs-RJLVrIWoLfQTKssZDoTMN3P19jc130_provenance.
- NP990994.RAabS4VfBL4vZEjOs-RJLVrIWoLfQTKssZDoTMN3P19jc130_assertion description "[Our studies thus demonstrate that the FLCN-FNIP complex deregulated in BHD syndrome is absolutely required for B-cell differentiation, and that it functions through both mTOR-dependent and independent pathways.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP990994.RAabS4VfBL4vZEjOs-RJLVrIWoLfQTKssZDoTMN3P19jc130_provenance.
- NP990994.RAabS4VfBL4vZEjOs-RJLVrIWoLfQTKssZDoTMN3P19jc130_assertion evidence source_evidence_literature NP990994.RAabS4VfBL4vZEjOs-RJLVrIWoLfQTKssZDoTMN3P19jc130_provenance.
- NP990994.RAabS4VfBL4vZEjOs-RJLVrIWoLfQTKssZDoTMN3P19jc130_assertion SIO_000772 22709692 NP990994.RAabS4VfBL4vZEjOs-RJLVrIWoLfQTKssZDoTMN3P19jc130_provenance.
- NP990994.RAabS4VfBL4vZEjOs-RJLVrIWoLfQTKssZDoTMN3P19jc130_assertion wasDerivedFrom befree-2016 NP990994.RAabS4VfBL4vZEjOs-RJLVrIWoLfQTKssZDoTMN3P19jc130_provenance.
- NP990994.RAabS4VfBL4vZEjOs-RJLVrIWoLfQTKssZDoTMN3P19jc130_assertion wasGeneratedBy ECO_0000203 NP990994.RAabS4VfBL4vZEjOs-RJLVrIWoLfQTKssZDoTMN3P19jc130_provenance.
- befree-2016 importedOn "2016-02-19" NP990994.RAabS4VfBL4vZEjOs-RJLVrIWoLfQTKssZDoTMN3P19jc130_provenance.