Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP434079.RArgw9VdlEXyCMpJaYo29flUFHyt2BJcmLnE8VfhjESLM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP434079.RArgw9VdlEXyCMpJaYo29flUFHyt2BJcmLnE8VfhjESLM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434079.RArgw9VdlEXyCMpJaYo29flUFHyt2BJcmLnE8VfhjESLM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434079.RArgw9VdlEXyCMpJaYo29flUFHyt2BJcmLnE8VfhjESLM130_provenance.
- NP434079.RArgw9VdlEXyCMpJaYo29flUFHyt2BJcmLnE8VfhjESLM130_assertion description "[The clinical presentation of the GRN A9D missense mutation is not restricted to behavioral variant frontotemporal dementia and may include aphasia, extrapyramidal features, and, notably, amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434079.RArgw9VdlEXyCMpJaYo29flUFHyt2BJcmLnE8VfhjESLM130_provenance.
- NP434079.RArgw9VdlEXyCMpJaYo29flUFHyt2BJcmLnE8VfhjESLM130_assertion evidence source_evidence_literature NP434079.RArgw9VdlEXyCMpJaYo29flUFHyt2BJcmLnE8VfhjESLM130_provenance.
- NP434079.RArgw9VdlEXyCMpJaYo29flUFHyt2BJcmLnE8VfhjESLM130_assertion SIO_000772 23596077 NP434079.RArgw9VdlEXyCMpJaYo29flUFHyt2BJcmLnE8VfhjESLM130_provenance.
- NP434079.RArgw9VdlEXyCMpJaYo29flUFHyt2BJcmLnE8VfhjESLM130_assertion wasDerivedFrom befree-20150227 NP434079.RArgw9VdlEXyCMpJaYo29flUFHyt2BJcmLnE8VfhjESLM130_provenance.
- NP434079.RArgw9VdlEXyCMpJaYo29flUFHyt2BJcmLnE8VfhjESLM130_assertion wasGeneratedBy ECO_0000203 NP434079.RArgw9VdlEXyCMpJaYo29flUFHyt2BJcmLnE8VfhjESLM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP434079.RArgw9VdlEXyCMpJaYo29flUFHyt2BJcmLnE8VfhjESLM130_provenance.