Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP384084.RA64bNUWWyGXEPyDLsLfoGXiuvYeAhk9PSiqONo-HsGK0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP384084.RA64bNUWWyGXEPyDLsLfoGXiuvYeAhk9PSiqONo-HsGK0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP384084.RA64bNUWWyGXEPyDLsLfoGXiuvYeAhk9PSiqONo-HsGK0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP384084.RA64bNUWWyGXEPyDLsLfoGXiuvYeAhk9PSiqONo-HsGK0130_provenance.
- NP384084.RA64bNUWWyGXEPyDLsLfoGXiuvYeAhk9PSiqONo-HsGK0130_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." NP384084.RA64bNUWWyGXEPyDLsLfoGXiuvYeAhk9PSiqONo-HsGK0130_provenance.
- NP384084.RA64bNUWWyGXEPyDLsLfoGXiuvYeAhk9PSiqONo-HsGK0130_assertion evidence source_evidence_literature NP384084.RA64bNUWWyGXEPyDLsLfoGXiuvYeAhk9PSiqONo-HsGK0130_provenance.
- NP384084.RA64bNUWWyGXEPyDLsLfoGXiuvYeAhk9PSiqONo-HsGK0130_assertion SIO_000772 23596077 NP384084.RA64bNUWWyGXEPyDLsLfoGXiuvYeAhk9PSiqONo-HsGK0130_provenance.
- NP384084.RA64bNUWWyGXEPyDLsLfoGXiuvYeAhk9PSiqONo-HsGK0130_assertion wasDerivedFrom befree-20140225 NP384084.RA64bNUWWyGXEPyDLsLfoGXiuvYeAhk9PSiqONo-HsGK0130_provenance.
- NP384084.RA64bNUWWyGXEPyDLsLfoGXiuvYeAhk9PSiqONo-HsGK0130_assertion wasGeneratedBy ECO_0000203 NP384084.RA64bNUWWyGXEPyDLsLfoGXiuvYeAhk9PSiqONo-HsGK0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP384084.RA64bNUWWyGXEPyDLsLfoGXiuvYeAhk9PSiqONo-HsGK0130_provenance.