Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP412643.RA2yLORYUZH1f1be3PHu-cMB6IN1Is9pM6rwMswgBsfWA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP412643.RA2yLORYUZH1f1be3PHu-cMB6IN1Is9pM6rwMswgBsfWA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP412643.RA2yLORYUZH1f1be3PHu-cMB6IN1Is9pM6rwMswgBsfWA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP412643.RA2yLORYUZH1f1be3PHu-cMB6IN1Is9pM6rwMswgBsfWA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP412643.RA2yLORYUZH1f1be3PHu-cMB6IN1Is9pM6rwMswgBsfWA130_provenance.
- NP412643.RA2yLORYUZH1f1be3PHu-cMB6IN1Is9pM6rwMswgBsfWA130_assertion wasGeneratedBy ECO_0000203 NP412643.RA2yLORYUZH1f1be3PHu-cMB6IN1Is9pM6rwMswgBsfWA130_provenance.
- NP412643.RA2yLORYUZH1f1be3PHu-cMB6IN1Is9pM6rwMswgBsfWA130_assertion wasDerivedFrom befree-20150227 NP412643.RA2yLORYUZH1f1be3PHu-cMB6IN1Is9pM6rwMswgBsfWA130_provenance.
- NP412643.RA2yLORYUZH1f1be3PHu-cMB6IN1Is9pM6rwMswgBsfWA130_assertion SIO_000772 23790110 NP412643.RA2yLORYUZH1f1be3PHu-cMB6IN1Is9pM6rwMswgBsfWA130_provenance.
- NP412643.RA2yLORYUZH1f1be3PHu-cMB6IN1Is9pM6rwMswgBsfWA130_assertion evidence source_evidence_literature NP412643.RA2yLORYUZH1f1be3PHu-cMB6IN1Is9pM6rwMswgBsfWA130_provenance.
- NP412643.RA2yLORYUZH1f1be3PHu-cMB6IN1Is9pM6rwMswgBsfWA130_assertion description "[Fragile X-associated tremor/ataxia syndrome (FXTAS) is a late-onset neurodegenerative disorder associated with FMR1 gene premutation alleles (55-200 CGG repeats).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412643.RA2yLORYUZH1f1be3PHu-cMB6IN1Is9pM6rwMswgBsfWA130_provenance.