Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1071602.RAG3iHNEQ-R2QC51T4my2E8_8hL-4URD1OfcPbaABp3s0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1071602.RAG3iHNEQ-R2QC51T4my2E8_8hL-4URD1OfcPbaABp3s0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1071602.RAG3iHNEQ-R2QC51T4my2E8_8hL-4URD1OfcPbaABp3s0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1071602.RAG3iHNEQ-R2QC51T4my2E8_8hL-4URD1OfcPbaABp3s0130_provenance.
- NP1071602.RAG3iHNEQ-R2QC51T4my2E8_8hL-4URD1OfcPbaABp3s0130_assertion description "[Mutations in the progranulin gene are known to cause diverse clinical syndromes, all attributed to frontotemporal lobar degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1071602.RAG3iHNEQ-R2QC51T4my2E8_8hL-4URD1OfcPbaABp3s0130_provenance.
- NP1071602.RAG3iHNEQ-R2QC51T4my2E8_8hL-4URD1OfcPbaABp3s0130_assertion evidence source_evidence_literature NP1071602.RAG3iHNEQ-R2QC51T4my2E8_8hL-4URD1OfcPbaABp3s0130_provenance.
- NP1071602.RAG3iHNEQ-R2QC51T4my2E8_8hL-4URD1OfcPbaABp3s0130_assertion SIO_000772 23609919 NP1071602.RAG3iHNEQ-R2QC51T4my2E8_8hL-4URD1OfcPbaABp3s0130_provenance.
- NP1071602.RAG3iHNEQ-R2QC51T4my2E8_8hL-4URD1OfcPbaABp3s0130_assertion wasDerivedFrom befree-2016 NP1071602.RAG3iHNEQ-R2QC51T4my2E8_8hL-4URD1OfcPbaABp3s0130_provenance.
- NP1071602.RAG3iHNEQ-R2QC51T4my2E8_8hL-4URD1OfcPbaABp3s0130_assertion wasGeneratedBy ECO_0000203 NP1071602.RAG3iHNEQ-R2QC51T4my2E8_8hL-4URD1OfcPbaABp3s0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1071602.RAG3iHNEQ-R2QC51T4my2E8_8hL-4URD1OfcPbaABp3s0130_provenance.