Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP54938.RA2o-FObH1fiXI2SROhgyFnNYVZjYj2sPce6F4cF7IQpU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP54938.RA2o-FObH1fiXI2SROhgyFnNYVZjYj2sPce6F4cF7IQpU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP54938.RA2o-FObH1fiXI2SROhgyFnNYVZjYj2sPce6F4cF7IQpU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP54938.RA2o-FObH1fiXI2SROhgyFnNYVZjYj2sPce6F4cF7IQpU130_provenance.
- NP54938.RA2o-FObH1fiXI2SROhgyFnNYVZjYj2sPce6F4cF7IQpU130_assertion description "[Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54938.RA2o-FObH1fiXI2SROhgyFnNYVZjYj2sPce6F4cF7IQpU130_provenance.
- NP54938.RA2o-FObH1fiXI2SROhgyFnNYVZjYj2sPce6F4cF7IQpU130_assertion evidence source_evidence_literature NP54938.RA2o-FObH1fiXI2SROhgyFnNYVZjYj2sPce6F4cF7IQpU130_provenance.
- NP54938.RA2o-FObH1fiXI2SROhgyFnNYVZjYj2sPce6F4cF7IQpU130_assertion SIO_000772 14740321 NP54938.RA2o-FObH1fiXI2SROhgyFnNYVZjYj2sPce6F4cF7IQpU130_provenance.
- NP54938.RA2o-FObH1fiXI2SROhgyFnNYVZjYj2sPce6F4cF7IQpU130_assertion wasDerivedFrom gad-20130706 NP54938.RA2o-FObH1fiXI2SROhgyFnNYVZjYj2sPce6F4cF7IQpU130_provenance.
- NP54938.RA2o-FObH1fiXI2SROhgyFnNYVZjYj2sPce6F4cF7IQpU130_assertion wasGeneratedBy ECO_0000203 NP54938.RA2o-FObH1fiXI2SROhgyFnNYVZjYj2sPce6F4cF7IQpU130_provenance.
- gad-20130706 importedOn "2013-07-06" NP54938.RA2o-FObH1fiXI2SROhgyFnNYVZjYj2sPce6F4cF7IQpU130_provenance.