Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP706501.RA6OXlRDtxKsYKtrw5sI6mwKV2RbFWePnY8CktIDKWFQY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP706501.RA6OXlRDtxKsYKtrw5sI6mwKV2RbFWePnY8CktIDKWFQY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP706501.RA6OXlRDtxKsYKtrw5sI6mwKV2RbFWePnY8CktIDKWFQY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP706501.RA6OXlRDtxKsYKtrw5sI6mwKV2RbFWePnY8CktIDKWFQY130_provenance.
- NP706501.RA6OXlRDtxKsYKtrw5sI6mwKV2RbFWePnY8CktIDKWFQY130_assertion description "[To evaluate the frequency of SQSTM1 mutations, we sequenced this gene in a cohort of patients with FTD or FTD-ALS, with no mutations in known FTD and ALS genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP706501.RA6OXlRDtxKsYKtrw5sI6mwKV2RbFWePnY8CktIDKWFQY130_provenance.
- NP706501.RA6OXlRDtxKsYKtrw5sI6mwKV2RbFWePnY8CktIDKWFQY130_assertion evidence source_evidence_literature NP706501.RA6OXlRDtxKsYKtrw5sI6mwKV2RbFWePnY8CktIDKWFQY130_provenance.
- NP706501.RA6OXlRDtxKsYKtrw5sI6mwKV2RbFWePnY8CktIDKWFQY130_assertion SIO_000772 24042580 NP706501.RA6OXlRDtxKsYKtrw5sI6mwKV2RbFWePnY8CktIDKWFQY130_provenance.
- NP706501.RA6OXlRDtxKsYKtrw5sI6mwKV2RbFWePnY8CktIDKWFQY130_assertion wasDerivedFrom befree-20150227 NP706501.RA6OXlRDtxKsYKtrw5sI6mwKV2RbFWePnY8CktIDKWFQY130_provenance.
- NP706501.RA6OXlRDtxKsYKtrw5sI6mwKV2RbFWePnY8CktIDKWFQY130_assertion wasGeneratedBy ECO_0000203 NP706501.RA6OXlRDtxKsYKtrw5sI6mwKV2RbFWePnY8CktIDKWFQY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP706501.RA6OXlRDtxKsYKtrw5sI6mwKV2RbFWePnY8CktIDKWFQY130_provenance.