@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP271865.RAVMG5t7C3OUiguk1hncSK30b7NiIWPcBaVpHTg8KavNM> .
@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:NP271865.RAVMG5t7C3OUiguk1hncSK30b7NiIWPcBaVpHTg8KavNM130_head {
  this: np:hasAssertion dgn-np:NP271865.RAVMG5t7C3OUiguk1hncSK30b7NiIWPcBaVpHTg8KavNM130_assertion;
    np:hasProvenance dgn-np:NP271865.RAVMG5t7C3OUiguk1hncSK30b7NiIWPcBaVpHTg8KavNM130_provenance;
    np:hasPublicationInfo dgn-np:NP271865.RAVMG5t7C3OUiguk1hncSK30b7NiIWPcBaVpHTg8KavNM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP271865.RAVMG5t7C3OUiguk1hncSK30b7NiIWPcBaVpHTg8KavNM130_assertion a np:Assertion .
  
  dgn-np:NP271865.RAVMG5t7C3OUiguk1hncSK30b7NiIWPcBaVpHTg8KavNM130_provenance a np:Provenance .
  
  dgn-np:NP271865.RAVMG5t7C3OUiguk1hncSK30b7NiIWPcBaVpHTg8KavNM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP271865.RAVMG5t7C3OUiguk1hncSK30b7NiIWPcBaVpHTg8KavNM130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  
  lld:C0151317 a ncit:C7057 .
  
  dgn-gda:DGN5c9e921a9cde809e512f492308aab1dd sio:SIO_000628 miriam-gene:1080, lld:C0151317;
    a sio:SIO_001121 .
}

dgn-np:NP271865.RAVMG5t7C3OUiguk1hncSK30b7NiIWPcBaVpHTg8KavNM130_provenance {
  dgn-np:NP271865.RAVMG5t7C3OUiguk1hncSK30b7NiIWPcBaVpHTg8KavNM130_assertion dcterms:description
      "[Cystic fibrosis (CF), which is among the most common life-shortening recessive illnesses, is caused by mutations of the CF transmembrane conductance regulator (CFTR) and typically involves chronic infection and progressive obstruction of the respiratory tract as well as pancreatic exocrine insufficiency.]. 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:18493878;
    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:NP271865.RAVMG5t7C3OUiguk1hncSK30b7NiIWPcBaVpHTg8KavNM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:33+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" .
}