@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP760296.RAC0aZO5GQ95tGA1cSzZjeLtA3mEYgPwZ7epOONpiYA1o> .
@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:NP760296.RAC0aZO5GQ95tGA1cSzZjeLtA3mEYgPwZ7epOONpiYA1o130_head {
  this: np:hasAssertion dgn-np:NP760296.RAC0aZO5GQ95tGA1cSzZjeLtA3mEYgPwZ7epOONpiYA1o130_assertion ;
    np:hasProvenance dgn-np:NP760296.RAC0aZO5GQ95tGA1cSzZjeLtA3mEYgPwZ7epOONpiYA1o130_provenance ;
    np:hasPublicationInfo dgn-np:NP760296.RAC0aZO5GQ95tGA1cSzZjeLtA3mEYgPwZ7epOONpiYA1o130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP760296.RAC0aZO5GQ95tGA1cSzZjeLtA3mEYgPwZ7epOONpiYA1o130_assertion a np:Assertion .
  dgn-np:NP760296.RAC0aZO5GQ95tGA1cSzZjeLtA3mEYgPwZ7epOONpiYA1o130_provenance a np:Provenance .
  dgn-np:NP760296.RAC0aZO5GQ95tGA1cSzZjeLtA3mEYgPwZ7epOONpiYA1o130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP760296.RAC0aZO5GQ95tGA1cSzZjeLtA3mEYgPwZ7epOONpiYA1o130_assertion {
  miriam-gene:5507 a ncit:C16612 .
  lld:C0000786 a ncit:C7057 .
  dgn-gda:DGNcc1fb6b2d17988373d85cf48de8e7cda sio:SIO_000628 miriam-gene:5507 , lld:C0000786 ;
    a sio:SIO_001121 .
}
dgn-np:NP760296.RAC0aZO5GQ95tGA1cSzZjeLtA3mEYgPwZ7epOONpiYA1o130_provenance {
  dgn-np:NP760296.RAC0aZO5GQ95tGA1cSzZjeLtA3mEYgPwZ7epOONpiYA1o130_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:NP760296.RAC0aZO5GQ95tGA1cSzZjeLtA3mEYgPwZ7epOONpiYA1o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:40+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" .
}