Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP980012.RA3Kulen_89CIPWXuEXdpnIkE-Z8xCfqYC4VizHW1O2vk130_assertion> ?p ?o ?g. }
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- NP980012.RA3Kulen_89CIPWXuEXdpnIkE-Z8xCfqYC4VizHW1O2vk130_assertion type Assertion NP980012.RA3Kulen_89CIPWXuEXdpnIkE-Z8xCfqYC4VizHW1O2vk130_head.
- NP980012.RA3Kulen_89CIPWXuEXdpnIkE-Z8xCfqYC4VizHW1O2vk130_assertion description "[Expansions of a hexanucleotide repeat (GGGGCC) in the noncoding region of the C9ORF72 gene are the most common cause of the familial form of ALS (C9-ALS), as well as frontotemporal lobar degeneration and other neurological diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP980012.RA3Kulen_89CIPWXuEXdpnIkE-Z8xCfqYC4VizHW1O2vk130_provenance.
- NP980012.RA3Kulen_89CIPWXuEXdpnIkE-Z8xCfqYC4VizHW1O2vk130_assertion evidence source_evidence_literature NP980012.RA3Kulen_89CIPWXuEXdpnIkE-Z8xCfqYC4VizHW1O2vk130_provenance.
- NP980012.RA3Kulen_89CIPWXuEXdpnIkE-Z8xCfqYC4VizHW1O2vk130_assertion SIO_000772 24154603 NP980012.RA3Kulen_89CIPWXuEXdpnIkE-Z8xCfqYC4VizHW1O2vk130_provenance.
- NP980012.RA3Kulen_89CIPWXuEXdpnIkE-Z8xCfqYC4VizHW1O2vk130_assertion wasDerivedFrom befree-20150227 NP980012.RA3Kulen_89CIPWXuEXdpnIkE-Z8xCfqYC4VizHW1O2vk130_provenance.
- NP980012.RA3Kulen_89CIPWXuEXdpnIkE-Z8xCfqYC4VizHW1O2vk130_assertion wasGeneratedBy ECO_0000203 NP980012.RA3Kulen_89CIPWXuEXdpnIkE-Z8xCfqYC4VizHW1O2vk130_provenance.