Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP593321.RAY4amXb_OpQRUGhXLXiMd23-shsU7mzMeWDzJ6aS84K0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP593321.RAY4amXb_OpQRUGhXLXiMd23-shsU7mzMeWDzJ6aS84K0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP593321.RAY4amXb_OpQRUGhXLXiMd23-shsU7mzMeWDzJ6aS84K0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP593321.RAY4amXb_OpQRUGhXLXiMd23-shsU7mzMeWDzJ6aS84K0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP593321.RAY4amXb_OpQRUGhXLXiMd23-shsU7mzMeWDzJ6aS84K0130_provenance.
- NP593321.RAY4amXb_OpQRUGhXLXiMd23-shsU7mzMeWDzJ6aS84K0130_assertion wasGeneratedBy ECO_0000203 NP593321.RAY4amXb_OpQRUGhXLXiMd23-shsU7mzMeWDzJ6aS84K0130_provenance.
- NP593321.RAY4amXb_OpQRUGhXLXiMd23-shsU7mzMeWDzJ6aS84K0130_assertion wasDerivedFrom befree-20150227 NP593321.RAY4amXb_OpQRUGhXLXiMd23-shsU7mzMeWDzJ6aS84K0130_provenance.
- NP593321.RAY4amXb_OpQRUGhXLXiMd23-shsU7mzMeWDzJ6aS84K0130_assertion SIO_000772 18042235 NP593321.RAY4amXb_OpQRUGhXLXiMd23-shsU7mzMeWDzJ6aS84K0130_provenance.
- NP593321.RAY4amXb_OpQRUGhXLXiMd23-shsU7mzMeWDzJ6aS84K0130_assertion evidence source_evidence_literature NP593321.RAY4amXb_OpQRUGhXLXiMd23-shsU7mzMeWDzJ6aS84K0130_provenance.
- NP593321.RAY4amXb_OpQRUGhXLXiMd23-shsU7mzMeWDzJ6aS84K0130_assertion description "[Eighty-nine patients with different neurodegenerative tau-related disorders, including 71 patients with frontotemporal lobar degeneration (FTLD), 12 with progressive supranuclear palsy (PSP) and 6 with corticobasal degeneration (CBD), were genotyped for the C276T single nucleotide polymorphism (SNP) in exon 29 of the nNOS gene and compared with 190 age-matched controls (CON).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP593321.RAY4amXb_OpQRUGhXLXiMd23-shsU7mzMeWDzJ6aS84K0130_provenance.