@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP798834.RAIoCdevp8WMbYCB233DBEjHNPjn3cHnqtLCmdzyA7vuY> .
@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:NP798834.RAIoCdevp8WMbYCB233DBEjHNPjn3cHnqtLCmdzyA7vuY130_head {
  this: np:hasAssertion dgn-np:NP798834.RAIoCdevp8WMbYCB233DBEjHNPjn3cHnqtLCmdzyA7vuY130_assertion;
    np:hasProvenance dgn-np:NP798834.RAIoCdevp8WMbYCB233DBEjHNPjn3cHnqtLCmdzyA7vuY130_provenance;
    np:hasPublicationInfo dgn-np:NP798834.RAIoCdevp8WMbYCB233DBEjHNPjn3cHnqtLCmdzyA7vuY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP798834.RAIoCdevp8WMbYCB233DBEjHNPjn3cHnqtLCmdzyA7vuY130_assertion a np:Assertion .
  
  dgn-np:NP798834.RAIoCdevp8WMbYCB233DBEjHNPjn3cHnqtLCmdzyA7vuY130_provenance a np:Provenance .
  
  dgn-np:NP798834.RAIoCdevp8WMbYCB233DBEjHNPjn3cHnqtLCmdzyA7vuY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP798834.RAIoCdevp8WMbYCB233DBEjHNPjn3cHnqtLCmdzyA7vuY130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  
  lld:C0023895 a ncit:C7057 .
  
  dgn-gda:DGN7c49f5100ae42788ac527d1138ab9366 sio:SIO_000628 miriam-gene:1080, lld:C0023895;
    a sio:SIO_001121 .
}

dgn-np:NP798834.RAIoCdevp8WMbYCB233DBEjHNPjn3cHnqtLCmdzyA7vuY130_provenance {
  dgn-np:NP798834.RAIoCdevp8WMbYCB233DBEjHNPjn3cHnqtLCmdzyA7vuY130_assertion dcterms:description
      "[A genotype-phenotype correlation has been observed only with pancreas status, while severity of lung involvement is not clearly related to the CFTR genotype, suggesting that this phenotype might be modulated by additional genetic or environmental factors; liver disease in general is not genetically determined.]. 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:8949420;
    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:NP798834.RAIoCdevp8WMbYCB233DBEjHNPjn3cHnqtLCmdzyA7vuY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:10+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" .
}