Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP95423.RAWSbTEDOEGLc5XhYvPJsZl_sCiA5fyIovPLnZDOL5X88130_assertion> ?p ?o ?g. }
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- NP95423.RAWSbTEDOEGLc5XhYvPJsZl_sCiA5fyIovPLnZDOL5X88130_assertion type Assertion NP95423.RAWSbTEDOEGLc5XhYvPJsZl_sCiA5fyIovPLnZDOL5X88130_head.
- NP95423.RAWSbTEDOEGLc5XhYvPJsZl_sCiA5fyIovPLnZDOL5X88130_assertion description "[The chromosome 9p21 locus is a major cause of familial ALS in the Finnish population. Our data suggest the presence of a founder mutation for chromosome 9p21-linked ALS. Furthermore, the overlap with the risk haplotype recently reported for frontotemporal dementia provides further evidence of a shared genetic cause for these two neurodegenerative diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95423.RAWSbTEDOEGLc5XhYvPJsZl_sCiA5fyIovPLnZDOL5X88130_provenance.
- NP95423.RAWSbTEDOEGLc5XhYvPJsZl_sCiA5fyIovPLnZDOL5X88130_assertion evidence source_evidence_literature NP95423.RAWSbTEDOEGLc5XhYvPJsZl_sCiA5fyIovPLnZDOL5X88130_provenance.
- NP95423.RAWSbTEDOEGLc5XhYvPJsZl_sCiA5fyIovPLnZDOL5X88130_assertion SIO_000772 20801718 NP95423.RAWSbTEDOEGLc5XhYvPJsZl_sCiA5fyIovPLnZDOL5X88130_provenance.
- NP95423.RAWSbTEDOEGLc5XhYvPJsZl_sCiA5fyIovPLnZDOL5X88130_assertion wasDerivedFrom gad-20130706 NP95423.RAWSbTEDOEGLc5XhYvPJsZl_sCiA5fyIovPLnZDOL5X88130_provenance.
- NP95423.RAWSbTEDOEGLc5XhYvPJsZl_sCiA5fyIovPLnZDOL5X88130_assertion wasGeneratedBy ECO_0000203 NP95423.RAWSbTEDOEGLc5XhYvPJsZl_sCiA5fyIovPLnZDOL5X88130_provenance.