@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP268520.RA07KvqUfmoei18eim12G1mz0TF3pje3vWZt-nEmFJGEY> .
@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:NP268520.RA07KvqUfmoei18eim12G1mz0TF3pje3vWZt-nEmFJGEY130_head {
  this: np:hasAssertion dgn-np:NP268520.RA07KvqUfmoei18eim12G1mz0TF3pje3vWZt-nEmFJGEY130_assertion ;
    np:hasProvenance dgn-np:NP268520.RA07KvqUfmoei18eim12G1mz0TF3pje3vWZt-nEmFJGEY130_provenance ;
    np:hasPublicationInfo dgn-np:NP268520.RA07KvqUfmoei18eim12G1mz0TF3pje3vWZt-nEmFJGEY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP268520.RA07KvqUfmoei18eim12G1mz0TF3pje3vWZt-nEmFJGEY130_assertion a np:Assertion .
  dgn-np:NP268520.RA07KvqUfmoei18eim12G1mz0TF3pje3vWZt-nEmFJGEY130_provenance a np:Provenance .
  dgn-np:NP268520.RA07KvqUfmoei18eim12G1mz0TF3pje3vWZt-nEmFJGEY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP268520.RA07KvqUfmoei18eim12G1mz0TF3pje3vWZt-nEmFJGEY130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  lld:C0010674 a ncit:C7057 .
  dgn-gda:DGN48ae0025bcb53323f815c60be704e5ff sio:SIO_000628 miriam-gene:1080 , lld:C0010674 ;
    a sio:SIO_001121 .
}
dgn-np:NP268520.RA07KvqUfmoei18eim12G1mz0TF3pje3vWZt-nEmFJGEY130_provenance {
  dgn-np:NP268520.RA07KvqUfmoei18eim12G1mz0TF3pje3vWZt-nEmFJGEY130_assertion dcterms:description "[A hypothetical cohort of 1000 women with singleton pregnancies and echogenic fetal bowel during the second trimester was used to determine the probability of cystic fibrosis when one cystic fibrosis transmembrane conductance regulator mutation was detected.]. 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:10576193 ;
    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:NP268520.RA07KvqUfmoei18eim12G1mz0TF3pje3vWZt-nEmFJGEY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:47+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" .
}