@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP988278.RAaPbC5FRnNYV5oW82tJgqQut6WK85Smt8HMO4mVm0pAc> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP988278.RAaPbC5FRnNYV5oW82tJgqQut6WK85Smt8HMO4mVm0pAc130_head {
  this: np:hasAssertion dgn-np:NP988278.RAaPbC5FRnNYV5oW82tJgqQut6WK85Smt8HMO4mVm0pAc130_assertion;
    np:hasProvenance dgn-np:NP988278.RAaPbC5FRnNYV5oW82tJgqQut6WK85Smt8HMO4mVm0pAc130_provenance;
    np:hasPublicationInfo dgn-np:NP988278.RAaPbC5FRnNYV5oW82tJgqQut6WK85Smt8HMO4mVm0pAc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP988278.RAaPbC5FRnNYV5oW82tJgqQut6WK85Smt8HMO4mVm0pAc130_assertion a np:Assertion .
  
  dgn-np:NP988278.RAaPbC5FRnNYV5oW82tJgqQut6WK85Smt8HMO4mVm0pAc130_provenance a np:Provenance .
  
  dgn-np:NP988278.RAaPbC5FRnNYV5oW82tJgqQut6WK85Smt8HMO4mVm0pAc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP988278.RAaPbC5FRnNYV5oW82tJgqQut6WK85Smt8HMO4mVm0pAc130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  
  lld:C0010674 a ncit:C7057 .
  
  dgn-gda:DGN2a814465cf8980d05a0239616bf70bb8 sio:SIO_000628 miriam-gene:1080, lld:C0010674;
    a sio:SIO_001121 .
}

dgn-np:NP988278.RAaPbC5FRnNYV5oW82tJgqQut6WK85Smt8HMO4mVm0pAc130_provenance {
  dgn-np:NP988278.RAaPbC5FRnNYV5oW82tJgqQut6WK85Smt8HMO4mVm0pAc130_assertion dcterms:description
      "[Genotype-phenotype correlations in cystic fibrosis (CF) may be difficult to establish because of phenotype variability, which is associated with certain CF transmembrane conductance regulator (CFTR) gene mutations and the existence of complex alleles.]. 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:22678879;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP988278.RAaPbC5FRnNYV5oW82tJgqQut6WK85Smt8HMO4mVm0pAc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:13+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}