Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1108184.RAe_ZuX4vbOe9afyxVRlxE0Mi7IXQuvzceGaE_ddCfI5c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1108184.RAe_ZuX4vbOe9afyxVRlxE0Mi7IXQuvzceGaE_ddCfI5c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1108184.RAe_ZuX4vbOe9afyxVRlxE0Mi7IXQuvzceGaE_ddCfI5c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1108184.RAe_ZuX4vbOe9afyxVRlxE0Mi7IXQuvzceGaE_ddCfI5c130_provenance.
- NP1108184.RAe_ZuX4vbOe9afyxVRlxE0Mi7IXQuvzceGaE_ddCfI5c130_assertion description "[The vast majority of FTLD and ALS are characterized by the abnormal accumulation of TDP-43, including genetic forms associated with mutations in the genes C9ORF72, GRN, TARDBP and VCP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1108184.RAe_ZuX4vbOe9afyxVRlxE0Mi7IXQuvzceGaE_ddCfI5c130_provenance.
- NP1108184.RAe_ZuX4vbOe9afyxVRlxE0Mi7IXQuvzceGaE_ddCfI5c130_assertion evidence source_evidence_literature NP1108184.RAe_ZuX4vbOe9afyxVRlxE0Mi7IXQuvzceGaE_ddCfI5c130_provenance.
- NP1108184.RAe_ZuX4vbOe9afyxVRlxE0Mi7IXQuvzceGaE_ddCfI5c130_assertion SIO_000772 24011641 NP1108184.RAe_ZuX4vbOe9afyxVRlxE0Mi7IXQuvzceGaE_ddCfI5c130_provenance.
- NP1108184.RAe_ZuX4vbOe9afyxVRlxE0Mi7IXQuvzceGaE_ddCfI5c130_assertion wasDerivedFrom befree-2016 NP1108184.RAe_ZuX4vbOe9afyxVRlxE0Mi7IXQuvzceGaE_ddCfI5c130_provenance.
- NP1108184.RAe_ZuX4vbOe9afyxVRlxE0Mi7IXQuvzceGaE_ddCfI5c130_assertion wasGeneratedBy ECO_0000203 NP1108184.RAe_ZuX4vbOe9afyxVRlxE0Mi7IXQuvzceGaE_ddCfI5c130_provenance.
- befree-2016 importedOn "2016-02-19" NP1108184.RAe_ZuX4vbOe9afyxVRlxE0Mi7IXQuvzceGaE_ddCfI5c130_provenance.