Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP963480.RACaFZAJIpQJnSpJeXqrji_yOvPSABRA5KM-E3a04URNs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP963480.RACaFZAJIpQJnSpJeXqrji_yOvPSABRA5KM-E3a04URNs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP963480.RACaFZAJIpQJnSpJeXqrji_yOvPSABRA5KM-E3a04URNs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP963480.RACaFZAJIpQJnSpJeXqrji_yOvPSABRA5KM-E3a04URNs130_provenance.
- NP963480.RACaFZAJIpQJnSpJeXqrji_yOvPSABRA5KM-E3a04URNs130_assertion description "[A total of 76 subjects, including 56 with a clinical diagnosis of behavioural variant frontotemporal dementia and a mutation in one of these genes (19 with C9ORF72 mutations, 25 with tau mutations and 12 with progranulin mutations) and 20 sporadic subjects with behavioural variant frontotemporal dementia (including 50% with amyotrophic lateral sclerosis), with magnetic resonance imaging were included in this study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963480.RACaFZAJIpQJnSpJeXqrji_yOvPSABRA5KM-E3a04URNs130_provenance.
- NP963480.RACaFZAJIpQJnSpJeXqrji_yOvPSABRA5KM-E3a04URNs130_assertion evidence source_evidence_literature NP963480.RACaFZAJIpQJnSpJeXqrji_yOvPSABRA5KM-E3a04URNs130_provenance.
- NP963480.RACaFZAJIpQJnSpJeXqrji_yOvPSABRA5KM-E3a04URNs130_assertion SIO_000772 22366795 NP963480.RACaFZAJIpQJnSpJeXqrji_yOvPSABRA5KM-E3a04URNs130_provenance.
- NP963480.RACaFZAJIpQJnSpJeXqrji_yOvPSABRA5KM-E3a04URNs130_assertion wasDerivedFrom befree-2016 NP963480.RACaFZAJIpQJnSpJeXqrji_yOvPSABRA5KM-E3a04URNs130_provenance.
- NP963480.RACaFZAJIpQJnSpJeXqrji_yOvPSABRA5KM-E3a04URNs130_assertion wasGeneratedBy ECO_0000203 NP963480.RACaFZAJIpQJnSpJeXqrji_yOvPSABRA5KM-E3a04URNs130_provenance.
- befree-2016 importedOn "2016-02-19" NP963480.RACaFZAJIpQJnSpJeXqrji_yOvPSABRA5KM-E3a04URNs130_provenance.