Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP618799.RAa1IWTMewtSJVXL4GMOQ8DMc1mzqZembf-WduM0O8HOQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP618799.RAa1IWTMewtSJVXL4GMOQ8DMc1mzqZembf-WduM0O8HOQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP618799.RAa1IWTMewtSJVXL4GMOQ8DMc1mzqZembf-WduM0O8HOQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP618799.RAa1IWTMewtSJVXL4GMOQ8DMc1mzqZembf-WduM0O8HOQ130_provenance.
- NP618799.RAa1IWTMewtSJVXL4GMOQ8DMc1mzqZembf-WduM0O8HOQ130_assertion description "[To investigate the role of the TDP-43 gene in sporadic forms of frontotemporal dementia (FTD), we genotyped 10 single nucleotide polymorphisms covering the entire TDP-43 genomic region, including the MASP2 gene in 173 patients with sporadic FTD (including 7 patients that were diagnosed with FTD and ALS) and 184 matched controls from Germany.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP618799.RAa1IWTMewtSJVXL4GMOQ8DMc1mzqZembf-WduM0O8HOQ130_provenance.
- NP618799.RAa1IWTMewtSJVXL4GMOQ8DMc1mzqZembf-WduM0O8HOQ130_assertion evidence source_evidence_literature NP618799.RAa1IWTMewtSJVXL4GMOQ8DMc1mzqZembf-WduM0O8HOQ130_provenance.
- NP618799.RAa1IWTMewtSJVXL4GMOQ8DMc1mzqZembf-WduM0O8HOQ130_assertion SIO_000772 17614162 NP618799.RAa1IWTMewtSJVXL4GMOQ8DMc1mzqZembf-WduM0O8HOQ130_provenance.
- NP618799.RAa1IWTMewtSJVXL4GMOQ8DMc1mzqZembf-WduM0O8HOQ130_assertion wasDerivedFrom befree-2016 NP618799.RAa1IWTMewtSJVXL4GMOQ8DMc1mzqZembf-WduM0O8HOQ130_provenance.
- NP618799.RAa1IWTMewtSJVXL4GMOQ8DMc1mzqZembf-WduM0O8HOQ130_assertion wasGeneratedBy ECO_0000203 NP618799.RAa1IWTMewtSJVXL4GMOQ8DMc1mzqZembf-WduM0O8HOQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP618799.RAa1IWTMewtSJVXL4GMOQ8DMc1mzqZembf-WduM0O8HOQ130_provenance.