@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP63517.RA2CqVka8GWL0L_edF3mVv2go2_1AwklyGLM4mcdGAwGU> .
@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:NP63517.RA2CqVka8GWL0L_edF3mVv2go2_1AwklyGLM4mcdGAwGU130_head {
  this: np:hasAssertion dgn-np:NP63517.RA2CqVka8GWL0L_edF3mVv2go2_1AwklyGLM4mcdGAwGU130_assertion ;
    np:hasProvenance dgn-np:NP63517.RA2CqVka8GWL0L_edF3mVv2go2_1AwklyGLM4mcdGAwGU130_provenance ;
    np:hasPublicationInfo dgn-np:NP63517.RA2CqVka8GWL0L_edF3mVv2go2_1AwklyGLM4mcdGAwGU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP63517.RA2CqVka8GWL0L_edF3mVv2go2_1AwklyGLM4mcdGAwGU130_assertion a np:Assertion .
  dgn-np:NP63517.RA2CqVka8GWL0L_edF3mVv2go2_1AwklyGLM4mcdGAwGU130_provenance a np:Provenance .
  dgn-np:NP63517.RA2CqVka8GWL0L_edF3mVv2go2_1AwklyGLM4mcdGAwGU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP63517.RA2CqVka8GWL0L_edF3mVv2go2_1AwklyGLM4mcdGAwGU130_assertion {
  miriam-gene:118 a ncit:C16612 .
  lld:C0151526 a ncit:C7057 .
  dgn-gda:DGN36e3655485958f2160485288bb9d21ec sio:SIO_000628 miriam-gene:118 , lld:C0151526 ;
    a sio:SIO_001122 .
}
dgn-np:NP63517.RA2CqVka8GWL0L_edF3mVv2go2_1AwklyGLM4mcdGAwGU130_provenance {
  dgn-np:NP63517.RA2CqVka8GWL0L_edF3mVv2go2_1AwklyGLM4mcdGAwGU130_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:NP63517.RA2CqVka8GWL0L_edF3mVv2go2_1AwklyGLM4mcdGAwGU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:30+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" .
}