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- source_evidence_literature type ECO_0000212 NP755621.RABatLgSUieVrnDqsoEtIMEeNoX-kj351yyVq9rNbH96E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP755621.RABatLgSUieVrnDqsoEtIMEeNoX-kj351yyVq9rNbH96E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP755621.RABatLgSUieVrnDqsoEtIMEeNoX-kj351yyVq9rNbH96E130_provenance.
- befree-2016 importedOn "2016-02-19" NP755621.RABatLgSUieVrnDqsoEtIMEeNoX-kj351yyVq9rNbH96E130_provenance.
- NP755621.RABatLgSUieVrnDqsoEtIMEeNoX-kj351yyVq9rNbH96E130_assertion wasGeneratedBy ECO_0000203 NP755621.RABatLgSUieVrnDqsoEtIMEeNoX-kj351yyVq9rNbH96E130_provenance.
- NP755621.RABatLgSUieVrnDqsoEtIMEeNoX-kj351yyVq9rNbH96E130_assertion wasDerivedFrom befree-2016 NP755621.RABatLgSUieVrnDqsoEtIMEeNoX-kj351yyVq9rNbH96E130_provenance.
- NP755621.RABatLgSUieVrnDqsoEtIMEeNoX-kj351yyVq9rNbH96E130_assertion SIO_000772 19657220 NP755621.RABatLgSUieVrnDqsoEtIMEeNoX-kj351yyVq9rNbH96E130_provenance.
- NP755621.RABatLgSUieVrnDqsoEtIMEeNoX-kj351yyVq9rNbH96E130_assertion evidence source_evidence_literature NP755621.RABatLgSUieVrnDqsoEtIMEeNoX-kj351yyVq9rNbH96E130_provenance.
- NP755621.RABatLgSUieVrnDqsoEtIMEeNoX-kj351yyVq9rNbH96E130_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." NP755621.RABatLgSUieVrnDqsoEtIMEeNoX-kj351yyVq9rNbH96E130_provenance.