@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP66007.RAJvTjnD09pE677B2BcY99fyP2a7AEkYQO6oDdymAPO10> .
@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:NP66007.RAJvTjnD09pE677B2BcY99fyP2a7AEkYQO6oDdymAPO10130_head {
  this: np:hasAssertion dgn-np:NP66007.RAJvTjnD09pE677B2BcY99fyP2a7AEkYQO6oDdymAPO10130_assertion;
    np:hasProvenance dgn-np:NP66007.RAJvTjnD09pE677B2BcY99fyP2a7AEkYQO6oDdymAPO10130_provenance;
    np:hasPublicationInfo dgn-np:NP66007.RAJvTjnD09pE677B2BcY99fyP2a7AEkYQO6oDdymAPO10130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP66007.RAJvTjnD09pE677B2BcY99fyP2a7AEkYQO6oDdymAPO10130_assertion a np:Assertion .
  
  dgn-np:NP66007.RAJvTjnD09pE677B2BcY99fyP2a7AEkYQO6oDdymAPO10130_provenance a np:Provenance .
  
  dgn-np:NP66007.RAJvTjnD09pE677B2BcY99fyP2a7AEkYQO6oDdymAPO10130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP66007.RAJvTjnD09pE677B2BcY99fyP2a7AEkYQO6oDdymAPO10130_assertion {
  miriam-gene:4843 a ncit:C16612 .
  
  lld:C0151526 a ncit:C7057 .
  
  dgn-gda:DGNb0ad1585469c8a4d204db75893eabae2 sio:SIO_000628 miriam-gene:4843, lld:C0151526;
    a sio:SIO_001122 .
}

dgn-np:NP66007.RAJvTjnD09pE677B2BcY99fyP2a7AEkYQO6oDdymAPO10130_provenance {
  dgn-np:NP66007.RAJvTjnD09pE677B2BcY99fyP2a7AEkYQO6oDdymAPO10130_assertion dcterms:description
      "[We confirm previous observations that variants of the beta adrenergic receptor and of nitric oxide synthase are associated with prematurity, and suggest that genetic variants of the placental antifibrinolytic plasminogen activator inhibitor-2, and thrombomodulin and alpha adducin may be contributors to risk of spontaneous preterm birth. LEVEL OF EVIDENCE: II]. 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:17267840;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP66007.RAJvTjnD09pE677B2BcY99fyP2a7AEkYQO6oDdymAPO10130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:31+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" .
}