@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP294382.RAShme_3vW7bp0nlakKh84_xSMhEVdO1YdeTyqs9n53xM> .
@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:NP294382.RAShme_3vW7bp0nlakKh84_xSMhEVdO1YdeTyqs9n53xM130_head {
  this: np:hasAssertion dgn-np:NP294382.RAShme_3vW7bp0nlakKh84_xSMhEVdO1YdeTyqs9n53xM130_assertion;
    np:hasProvenance dgn-np:NP294382.RAShme_3vW7bp0nlakKh84_xSMhEVdO1YdeTyqs9n53xM130_provenance;
    np:hasPublicationInfo dgn-np:NP294382.RAShme_3vW7bp0nlakKh84_xSMhEVdO1YdeTyqs9n53xM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP294382.RAShme_3vW7bp0nlakKh84_xSMhEVdO1YdeTyqs9n53xM130_assertion a np:Assertion .
  
  dgn-np:NP294382.RAShme_3vW7bp0nlakKh84_xSMhEVdO1YdeTyqs9n53xM130_provenance a np:Provenance .
  
  dgn-np:NP294382.RAShme_3vW7bp0nlakKh84_xSMhEVdO1YdeTyqs9n53xM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP294382.RAShme_3vW7bp0nlakKh84_xSMhEVdO1YdeTyqs9n53xM130_assertion {
  miriam-gene:5053 a ncit:C16612 .
  
  lld:C0011849 a ncit:C7057 .
  
  dgn-gda:DGNe0cdbddaf93c815f53768144daa36868 sio:SIO_000628 miriam-gene:5053, lld:C0011849;
    a sio:SIO_001121 .
}

dgn-np:NP294382.RAShme_3vW7bp0nlakKh84_xSMhEVdO1YdeTyqs9n53xM130_provenance {
  dgn-np:NP294382.RAShme_3vW7bp0nlakKh84_xSMhEVdO1YdeTyqs9n53xM130_assertion dcterms:description
      "[Nevertheless, there is fair agreement that a variety of factors may increase risk for SAB or RAB, including advanced maternal age, single gene mutations such as PKU or G6PD deficiency, structural abnormalities of the uterus, poorly controlled diabetes, antiphospholipid syndrome, and smoking.]. 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:11355791;
    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:NP294382.RAShme_3vW7bp0nlakKh84_xSMhEVdO1YdeTyqs9n53xM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:47+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" .
}