Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP634821.RAuB_fNUza5ckERUcwQas9WR5q5t6zB6JV0NKWx19fxNw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP634821.RAuB_fNUza5ckERUcwQas9WR5q5t6zB6JV0NKWx19fxNw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP634821.RAuB_fNUza5ckERUcwQas9WR5q5t6zB6JV0NKWx19fxNw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP634821.RAuB_fNUza5ckERUcwQas9WR5q5t6zB6JV0NKWx19fxNw130_provenance.
- NP634821.RAuB_fNUza5ckERUcwQas9WR5q5t6zB6JV0NKWx19fxNw130_assertion description "[The objective of this study was to identify the frequency of REEP1 mutations in both autosomal dominant HSP (ADHSP) and sporadic spastic paraparesis (SSP) cases and to analyse the genotype/phenotype correlation of mutations so far described in REEP1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP634821.RAuB_fNUza5ckERUcwQas9WR5q5t6zB6JV0NKWx19fxNw130_provenance.
- NP634821.RAuB_fNUza5ckERUcwQas9WR5q5t6zB6JV0NKWx19fxNw130_assertion evidence source_evidence_literature NP634821.RAuB_fNUza5ckERUcwQas9WR5q5t6zB6JV0NKWx19fxNw130_provenance.
- NP634821.RAuB_fNUza5ckERUcwQas9WR5q5t6zB6JV0NKWx19fxNw130_assertion SIO_000772 19034539 NP634821.RAuB_fNUza5ckERUcwQas9WR5q5t6zB6JV0NKWx19fxNw130_provenance.
- NP634821.RAuB_fNUza5ckERUcwQas9WR5q5t6zB6JV0NKWx19fxNw130_assertion wasDerivedFrom befree-20140225 NP634821.RAuB_fNUza5ckERUcwQas9WR5q5t6zB6JV0NKWx19fxNw130_provenance.
- NP634821.RAuB_fNUza5ckERUcwQas9WR5q5t6zB6JV0NKWx19fxNw130_assertion wasGeneratedBy ECO_0000203 NP634821.RAuB_fNUza5ckERUcwQas9WR5q5t6zB6JV0NKWx19fxNw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP634821.RAuB_fNUza5ckERUcwQas9WR5q5t6zB6JV0NKWx19fxNw130_provenance.