Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP980012.RA3Kulen_89CIPWXuEXdpnIkE-Z8xCfqYC4VizHW1O2vk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP980012.RA3Kulen_89CIPWXuEXdpnIkE-Z8xCfqYC4VizHW1O2vk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP980012.RA3Kulen_89CIPWXuEXdpnIkE-Z8xCfqYC4VizHW1O2vk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP980012.RA3Kulen_89CIPWXuEXdpnIkE-Z8xCfqYC4VizHW1O2vk130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP980012.RA3Kulen_89CIPWXuEXdpnIkE-Z8xCfqYC4VizHW1O2vk130_provenance.