@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_head {
  this: np:hasAssertion dgn-np:NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_assertion;
    np:hasProvenance dgn-np:NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_provenance;
    np:hasPublicationInfo dgn-np:NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_assertion a np:Assertion .
  
  dgn-np:NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_provenance a np:Provenance .
  
  dgn-np:NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_assertion {
  miriam-gene:6690 a ncit:C16612 .
  
  lld:C0011847 a ncit:C7057 .
  
  dgn-gda:DGN43c9d23c5ff96de3d7bc0b20810b78c6 sio:SIO_000628 miriam-gene:6690, lld:C0011847;
    a sio:SIO_001121 .
}

dgn-np:NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_provenance {
  dgn-np:NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_assertion dcterms:description
      "[We dichotomized the whole cohort based on the presence or absence of N34S SPINK1 and L26V CTSB mutations and further subdivided them into TCP and FCPD patients and compared the distribution of TCF7L2 variants between them.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:18706099;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:59+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}