Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP979614.RAgVo8jy9uB25pbs9iV4G71xwiKz2mU00EfcPgV2g3Oak130_assertion> ?p ?o ?g. }
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- NP979614.RAgVo8jy9uB25pbs9iV4G71xwiKz2mU00EfcPgV2g3Oak130_assertion type Assertion NP979614.RAgVo8jy9uB25pbs9iV4G71xwiKz2mU00EfcPgV2g3Oak130_head.
- NP979614.RAgVo8jy9uB25pbs9iV4G71xwiKz2mU00EfcPgV2g3Oak130_assertion description "[Rare mutations in the gene encoding for tau (MAPT, microtubule-associated protein tau) cause frontotemporal dementia-spectrum (FTD-s) disorders, including FTD, progressive supranuclear palsy (PSP) and corticobasal syndrome, and a common extended haplotype spanning across the MAPT locus is associated with increased risk of PSP and Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP979614.RAgVo8jy9uB25pbs9iV4G71xwiKz2mU00EfcPgV2g3Oak130_provenance.
- NP979614.RAgVo8jy9uB25pbs9iV4G71xwiKz2mU00EfcPgV2g3Oak130_assertion evidence source_evidence_literature NP979614.RAgVo8jy9uB25pbs9iV4G71xwiKz2mU00EfcPgV2g3Oak130_provenance.
- NP979614.RAgVo8jy9uB25pbs9iV4G71xwiKz2mU00EfcPgV2g3Oak130_assertion SIO_000772 22556362 NP979614.RAgVo8jy9uB25pbs9iV4G71xwiKz2mU00EfcPgV2g3Oak130_provenance.
- NP979614.RAgVo8jy9uB25pbs9iV4G71xwiKz2mU00EfcPgV2g3Oak130_assertion wasDerivedFrom befree-2016 NP979614.RAgVo8jy9uB25pbs9iV4G71xwiKz2mU00EfcPgV2g3Oak130_provenance.
- NP979614.RAgVo8jy9uB25pbs9iV4G71xwiKz2mU00EfcPgV2g3Oak130_assertion wasGeneratedBy ECO_0000203 NP979614.RAgVo8jy9uB25pbs9iV4G71xwiKz2mU00EfcPgV2g3Oak130_provenance.