@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP624474.RAncfv4WliBVM7rfHO8QKR3aSpa7VvM1izSBWrNz559jA> .
@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:NP624474.RAncfv4WliBVM7rfHO8QKR3aSpa7VvM1izSBWrNz559jA130_head {
  this: np:hasAssertion dgn-np:NP624474.RAncfv4WliBVM7rfHO8QKR3aSpa7VvM1izSBWrNz559jA130_assertion;
    np:hasProvenance dgn-np:NP624474.RAncfv4WliBVM7rfHO8QKR3aSpa7VvM1izSBWrNz559jA130_provenance;
    np:hasPublicationInfo dgn-np:NP624474.RAncfv4WliBVM7rfHO8QKR3aSpa7VvM1izSBWrNz559jA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP624474.RAncfv4WliBVM7rfHO8QKR3aSpa7VvM1izSBWrNz559jA130_assertion a np:Assertion .
  
  dgn-np:NP624474.RAncfv4WliBVM7rfHO8QKR3aSpa7VvM1izSBWrNz559jA130_provenance a np:Provenance .
  
  dgn-np:NP624474.RAncfv4WliBVM7rfHO8QKR3aSpa7VvM1izSBWrNz559jA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP624474.RAncfv4WliBVM7rfHO8QKR3aSpa7VvM1izSBWrNz559jA130_assertion {
  miriam-gene:288 a ncit:C16612 .
  
  lld:C0006012 a ncit:C7057 .
  
  dgn-gda:DGNd5a864ec49eeee96f71ca3912ed15825 sio:SIO_000628 miriam-gene:288, lld:C0006012;
    a sio:SIO_001121 .
}

dgn-np:NP624474.RAncfv4WliBVM7rfHO8QKR3aSpa7VvM1izSBWrNz559jA130_provenance {
  dgn-np:NP624474.RAncfv4WliBVM7rfHO8QKR3aSpa7VvM1izSBWrNz559jA130_assertion dcterms:description
      "[While we could not confirm an association of ANK3, CACNA1C, and EGFR with BPD, 10 SNPs in DGKH, CMTM8, and NPAS3 were nominally associated with disease, with two DGKH markers surviving correction for multiple testing.]. 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:21654738;
    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:NP624474.RAncfv4WliBVM7rfHO8QKR3aSpa7VvM1izSBWrNz559jA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:17+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" .
}