Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1401024.RAepVt-sN0dhIAx0NlFM6uC7DKqcH55vZd3aRo9yc0AA8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1401024.RAepVt-sN0dhIAx0NlFM6uC7DKqcH55vZd3aRo9yc0AA8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1401024.RAepVt-sN0dhIAx0NlFM6uC7DKqcH55vZd3aRo9yc0AA8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1401024.RAepVt-sN0dhIAx0NlFM6uC7DKqcH55vZd3aRo9yc0AA8130_provenance.
- NP1401024.RAepVt-sN0dhIAx0NlFM6uC7DKqcH55vZd3aRo9yc0AA8130_assertion description "[We studied 133 Japanese patients with retinal dystrophies to detect peripherin/RDS (retinal degeneration slow) gene defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1401024.RAepVt-sN0dhIAx0NlFM6uC7DKqcH55vZd3aRo9yc0AA8130_provenance.
- NP1401024.RAepVt-sN0dhIAx0NlFM6uC7DKqcH55vZd3aRo9yc0AA8130_assertion evidence source_evidence_literature NP1401024.RAepVt-sN0dhIAx0NlFM6uC7DKqcH55vZd3aRo9yc0AA8130_provenance.
- NP1401024.RAepVt-sN0dhIAx0NlFM6uC7DKqcH55vZd3aRo9yc0AA8130_assertion SIO_000772 9690896 NP1401024.RAepVt-sN0dhIAx0NlFM6uC7DKqcH55vZd3aRo9yc0AA8130_provenance.
- NP1401024.RAepVt-sN0dhIAx0NlFM6uC7DKqcH55vZd3aRo9yc0AA8130_assertion wasDerivedFrom befree-2016 NP1401024.RAepVt-sN0dhIAx0NlFM6uC7DKqcH55vZd3aRo9yc0AA8130_provenance.
- NP1401024.RAepVt-sN0dhIAx0NlFM6uC7DKqcH55vZd3aRo9yc0AA8130_assertion wasGeneratedBy ECO_0000203 NP1401024.RAepVt-sN0dhIAx0NlFM6uC7DKqcH55vZd3aRo9yc0AA8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1401024.RAepVt-sN0dhIAx0NlFM6uC7DKqcH55vZd3aRo9yc0AA8130_provenance.