@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP339108.RA6eQpr2QVAlpdZRKag97atUILwdpcHA74Q5Lv1TBn5_Q> .
@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:NP339108.RA6eQpr2QVAlpdZRKag97atUILwdpcHA74Q5Lv1TBn5_Q130_head {
  this: np:hasAssertion dgn-np:NP339108.RA6eQpr2QVAlpdZRKag97atUILwdpcHA74Q5Lv1TBn5_Q130_assertion ;
    np:hasProvenance dgn-np:NP339108.RA6eQpr2QVAlpdZRKag97atUILwdpcHA74Q5Lv1TBn5_Q130_provenance ;
    np:hasPublicationInfo dgn-np:NP339108.RA6eQpr2QVAlpdZRKag97atUILwdpcHA74Q5Lv1TBn5_Q130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP339108.RA6eQpr2QVAlpdZRKag97atUILwdpcHA74Q5Lv1TBn5_Q130_assertion a np:Assertion .
  dgn-np:NP339108.RA6eQpr2QVAlpdZRKag97atUILwdpcHA74Q5Lv1TBn5_Q130_provenance a np:Provenance .
  dgn-np:NP339108.RA6eQpr2QVAlpdZRKag97atUILwdpcHA74Q5Lv1TBn5_Q130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP339108.RA6eQpr2QVAlpdZRKag97atUILwdpcHA74Q5Lv1TBn5_Q130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  lld:C0006267 a ncit:C7057 .
  dgn-gda:DGN76d87ca4a4890dffc1052a5e0d403fec sio:SIO_000628 miriam-gene:1080 , lld:C0006267 ;
    a sio:SIO_001121 .
}
dgn-np:NP339108.RA6eQpr2QVAlpdZRKag97atUILwdpcHA74Q5Lv1TBn5_Q130_provenance {
  dgn-np:NP339108.RA6eQpr2QVAlpdZRKag97atUILwdpcHA74Q5Lv1TBn5_Q130_assertion dcterms:description "[The number of requests is growing, owing to the increasingly wide range of recognized CFTR gene diseases (cystic fibrosis, congenital bilateral absence of the vas deferens, disseminated bronchiectasis, allergic bronchopulmonary aspergillosis and chronic pancreatitis), and the availability of efficient molecular tools for detecting mutations.]. 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:10649490 ;
    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:NP339108.RA6eQpr2QVAlpdZRKag97atUILwdpcHA74Q5Lv1TBn5_Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:19+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" .
}