Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP588697.RABPA0ngMWwa1mkm7m6oEe3s4iQk6KD7TfV8KbRxaOAi0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP588697.RABPA0ngMWwa1mkm7m6oEe3s4iQk6KD7TfV8KbRxaOAi0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP588697.RABPA0ngMWwa1mkm7m6oEe3s4iQk6KD7TfV8KbRxaOAi0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP588697.RABPA0ngMWwa1mkm7m6oEe3s4iQk6KD7TfV8KbRxaOAi0130_provenance.
- NP588697.RABPA0ngMWwa1mkm7m6oEe3s4iQk6KD7TfV8KbRxaOAi0130_assertion description "[To examine whether C9ORF72 expansions could be involved in early-onset Alzheimer's disease (EOAD), we genotyped the hexanucleotide repeat region in a large cohort of 114 EOAD patients who all had positive AD cerebrospinal fluid (CSF) biomarkers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588697.RABPA0ngMWwa1mkm7m6oEe3s4iQk6KD7TfV8KbRxaOAi0130_provenance.
- NP588697.RABPA0ngMWwa1mkm7m6oEe3s4iQk6KD7TfV8KbRxaOAi0130_assertion evidence source_evidence_literature NP588697.RABPA0ngMWwa1mkm7m6oEe3s4iQk6KD7TfV8KbRxaOAi0130_provenance.
- NP588697.RABPA0ngMWwa1mkm7m6oEe3s4iQk6KD7TfV8KbRxaOAi0130_assertion SIO_000772 22766732 NP588697.RABPA0ngMWwa1mkm7m6oEe3s4iQk6KD7TfV8KbRxaOAi0130_provenance.
- NP588697.RABPA0ngMWwa1mkm7m6oEe3s4iQk6KD7TfV8KbRxaOAi0130_assertion wasDerivedFrom befree-20140225 NP588697.RABPA0ngMWwa1mkm7m6oEe3s4iQk6KD7TfV8KbRxaOAi0130_provenance.
- NP588697.RABPA0ngMWwa1mkm7m6oEe3s4iQk6KD7TfV8KbRxaOAi0130_assertion wasGeneratedBy ECO_0000203 NP588697.RABPA0ngMWwa1mkm7m6oEe3s4iQk6KD7TfV8KbRxaOAi0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP588697.RABPA0ngMWwa1mkm7m6oEe3s4iQk6KD7TfV8KbRxaOAi0130_provenance.