@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE> .
@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/v3.0.0/void/> .
dgn-np:NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_head {
  this: np:hasAssertion dgn-np:NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_assertion ;
    np:hasProvenance dgn-np:NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_provenance ;
    np:hasPublicationInfo dgn-np:NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_assertion a np:Assertion .
  dgn-np:NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_provenance a np:Provenance .
  dgn-np:NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_assertion {
  miriam-gene:6462 a ncit:C16612 .
  lld:C0021361 a ncit:C7057 .
  dgn-gda:DGN9b8a76f42e9566ffc1331836faef0549 sio:SIO_000628 miriam-gene:6462 , lld:C0021361 ;
    a sio:SIO_001122 .
}
dgn-np:NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_provenance {
  dgn-np:NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_assertion dcterms:description "[Candidate associations were identified between recurrent miscarriage and genetic variation within ESR2, PRLR, GCCR and ACVR1 genes. Independent confirmation of these results is needed, as limitations of this study include the heterogeneous etiology of rec]. 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:20716560 ;
    prov:wasDerivedFrom dgn-void:gad-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_publicationInfo {
  this: dcterms:created "2015-08-25T14:39:05+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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}