Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1069485.RAT8MgNcPMPsDw0NVWdKQZyUWKPGCaEVtYwj3Alh-3sKM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1069485.RAT8MgNcPMPsDw0NVWdKQZyUWKPGCaEVtYwj3Alh-3sKM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1069485.RAT8MgNcPMPsDw0NVWdKQZyUWKPGCaEVtYwj3Alh-3sKM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1069485.RAT8MgNcPMPsDw0NVWdKQZyUWKPGCaEVtYwj3Alh-3sKM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1069485.RAT8MgNcPMPsDw0NVWdKQZyUWKPGCaEVtYwj3Alh-3sKM130_provenance.
- NP1069485.RAT8MgNcPMPsDw0NVWdKQZyUWKPGCaEVtYwj3Alh-3sKM130_assertion wasGeneratedBy ECO_0000203 NP1069485.RAT8MgNcPMPsDw0NVWdKQZyUWKPGCaEVtYwj3Alh-3sKM130_provenance.
- NP1069485.RAT8MgNcPMPsDw0NVWdKQZyUWKPGCaEVtYwj3Alh-3sKM130_assertion wasDerivedFrom befree-2016 NP1069485.RAT8MgNcPMPsDw0NVWdKQZyUWKPGCaEVtYwj3Alh-3sKM130_provenance.
- NP1069485.RAT8MgNcPMPsDw0NVWdKQZyUWKPGCaEVtYwj3Alh-3sKM130_assertion SIO_000772 23588422 NP1069485.RAT8MgNcPMPsDw0NVWdKQZyUWKPGCaEVtYwj3Alh-3sKM130_provenance.
- NP1069485.RAT8MgNcPMPsDw0NVWdKQZyUWKPGCaEVtYwj3Alh-3sKM130_assertion evidence source_evidence_literature NP1069485.RAT8MgNcPMPsDw0NVWdKQZyUWKPGCaEVtYwj3Alh-3sKM130_provenance.
- NP1069485.RAT8MgNcPMPsDw0NVWdKQZyUWKPGCaEVtYwj3Alh-3sKM130_assertion description "[Hexanucleotide repeat expansions in the chromosome 9 open reading frame 72 (C9orf72) gene underlie a significant fraction of frontotemporal dementia and amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1069485.RAT8MgNcPMPsDw0NVWdKQZyUWKPGCaEVtYwj3Alh-3sKM130_provenance.