@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP289486.RAtxnJWV31qYWnJnHdUyLlBsSjaNW-l_YOQ1vk0uMcuvc> .
@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:NP289486.RAtxnJWV31qYWnJnHdUyLlBsSjaNW-l_YOQ1vk0uMcuvc130_head {
  this: np:hasAssertion dgn-np:NP289486.RAtxnJWV31qYWnJnHdUyLlBsSjaNW-l_YOQ1vk0uMcuvc130_assertion ;
    np:hasProvenance dgn-np:NP289486.RAtxnJWV31qYWnJnHdUyLlBsSjaNW-l_YOQ1vk0uMcuvc130_provenance ;
    np:hasPublicationInfo dgn-np:NP289486.RAtxnJWV31qYWnJnHdUyLlBsSjaNW-l_YOQ1vk0uMcuvc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP289486.RAtxnJWV31qYWnJnHdUyLlBsSjaNW-l_YOQ1vk0uMcuvc130_assertion a np:Assertion .
  dgn-np:NP289486.RAtxnJWV31qYWnJnHdUyLlBsSjaNW-l_YOQ1vk0uMcuvc130_provenance a np:Provenance .
  dgn-np:NP289486.RAtxnJWV31qYWnJnHdUyLlBsSjaNW-l_YOQ1vk0uMcuvc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP289486.RAtxnJWV31qYWnJnHdUyLlBsSjaNW-l_YOQ1vk0uMcuvc130_assertion {
  miriam-gene:3126 a ncit:C16612 .
  lld:C0000786 a ncit:C7057 .
  dgn-gda:DGN95247ab04095353050181525396e5840 sio:SIO_000628 miriam-gene:3126 , lld:C0000786 ;
    a sio:SIO_001121 .
}
dgn-np:NP289486.RAtxnJWV31qYWnJnHdUyLlBsSjaNW-l_YOQ1vk0uMcuvc130_provenance {
  dgn-np:NP289486.RAtxnJWV31qYWnJnHdUyLlBsSjaNW-l_YOQ1vk0uMcuvc130_assertion dcterms:description "[To determine if a 14-bp deletion/insertion polymorphism in the 3'-untranslated region of exon 8 of the gene encoding human leukocyte antigen (HLA)-G in a homozygous form is associated with repeated, unsuccessful in vitro fertilization (IVF) treatments, and with increased risk of recurrent spontaneous abortions (RSA), 29 white women undergoing IVF treatments, 61 RSA women and 93 fertile controls were HLA-G genotype.]. 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:15191524 ;
    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:NP289486.RAtxnJWV31qYWnJnHdUyLlBsSjaNW-l_YOQ1vk0uMcuvc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:44+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" .
}