@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP403589.RA6ROuHAFAObzHsf3HtmvXL_o9f2972JqO2IA12glgCQw> .
@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:NP403589.RA6ROuHAFAObzHsf3HtmvXL_o9f2972JqO2IA12glgCQw130_head {
  this: np:hasAssertion dgn-np:NP403589.RA6ROuHAFAObzHsf3HtmvXL_o9f2972JqO2IA12glgCQw130_assertion;
    np:hasProvenance dgn-np:NP403589.RA6ROuHAFAObzHsf3HtmvXL_o9f2972JqO2IA12glgCQw130_provenance;
    np:hasPublicationInfo dgn-np:NP403589.RA6ROuHAFAObzHsf3HtmvXL_o9f2972JqO2IA12glgCQw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP403589.RA6ROuHAFAObzHsf3HtmvXL_o9f2972JqO2IA12glgCQw130_assertion a np:Assertion .
  
  dgn-np:NP403589.RA6ROuHAFAObzHsf3HtmvXL_o9f2972JqO2IA12glgCQw130_provenance a np:Provenance .
  
  dgn-np:NP403589.RA6ROuHAFAObzHsf3HtmvXL_o9f2972JqO2IA12glgCQw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP403589.RA6ROuHAFAObzHsf3HtmvXL_o9f2972JqO2IA12glgCQw130_assertion {
  miriam-gene:2153 a ncit:C16612 .
  
  lld:C0000786 a ncit:C7057 .
  
  dgn-gda:DGNda6018e5254c6ed8f9d5dedf540287da sio:SIO_000628 miriam-gene:2153, lld:C0000786;
    a sio:SIO_001121 .
}

dgn-np:NP403589.RA6ROuHAFAObzHsf3HtmvXL_o9f2972JqO2IA12glgCQw130_provenance {
  dgn-np:NP403589.RA6ROuHAFAObzHsf3HtmvXL_o9f2972JqO2IA12glgCQw130_assertion dcterms:description
      "[We determined (i) the prevalence of three thrombophilic mutations [factor V Leiden (FVL), prothrombin G20210A (PTG) and methylenetetrahydrofolate reductase (MTHFR) C677T] amongst 357 Caucasian couples with RM and 68 parous Caucasian couples with no history of miscarriage and (ii) the prospective outcome of untreated pregnancies amongst couples with RM in which either partner carried a thrombophilic mutation.]. 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:16431900;
    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:NP403589.RA6ROuHAFAObzHsf3HtmvXL_o9f2972JqO2IA12glgCQw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:00+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" .
}