Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP755618.RA-IEqGVxO2dQpCO34-zX5hc1xQ7NlyurRfigNry4x1E0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP755618.RA-IEqGVxO2dQpCO34-zX5hc1xQ7NlyurRfigNry4x1E0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP755618.RA-IEqGVxO2dQpCO34-zX5hc1xQ7NlyurRfigNry4x1E0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP755618.RA-IEqGVxO2dQpCO34-zX5hc1xQ7NlyurRfigNry4x1E0130_provenance.
- befree-2016 importedOn "2016-02-19" NP755618.RA-IEqGVxO2dQpCO34-zX5hc1xQ7NlyurRfigNry4x1E0130_provenance.
- NP755618.RA-IEqGVxO2dQpCO34-zX5hc1xQ7NlyurRfigNry4x1E0130_assertion wasGeneratedBy ECO_0000203 NP755618.RA-IEqGVxO2dQpCO34-zX5hc1xQ7NlyurRfigNry4x1E0130_provenance.
- NP755618.RA-IEqGVxO2dQpCO34-zX5hc1xQ7NlyurRfigNry4x1E0130_assertion wasDerivedFrom befree-2016 NP755618.RA-IEqGVxO2dQpCO34-zX5hc1xQ7NlyurRfigNry4x1E0130_provenance.
- NP755618.RA-IEqGVxO2dQpCO34-zX5hc1xQ7NlyurRfigNry4x1E0130_assertion SIO_000772 19657220 NP755618.RA-IEqGVxO2dQpCO34-zX5hc1xQ7NlyurRfigNry4x1E0130_provenance.
- NP755618.RA-IEqGVxO2dQpCO34-zX5hc1xQ7NlyurRfigNry4x1E0130_assertion evidence source_evidence_literature NP755618.RA-IEqGVxO2dQpCO34-zX5hc1xQ7NlyurRfigNry4x1E0130_provenance.
- NP755618.RA-IEqGVxO2dQpCO34-zX5hc1xQ7NlyurRfigNry4x1E0130_assertion description "[The aim of this study was to determine for the first time the significance of PRSS1, SPINK1 mutations and genetic variants of AAT in a group of Spanish patients with CP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755618.RA-IEqGVxO2dQpCO34-zX5hc1xQ7NlyurRfigNry4x1E0130_provenance.