@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP820706.RAzd4EkGxapVel7UgOK8I50pPtCoDxOSgKNIWeeEZyVXQ> .
@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:NP820706.RAzd4EkGxapVel7UgOK8I50pPtCoDxOSgKNIWeeEZyVXQ130_head {
  this: np:hasAssertion dgn-np:NP820706.RAzd4EkGxapVel7UgOK8I50pPtCoDxOSgKNIWeeEZyVXQ130_assertion ;
    np:hasProvenance dgn-np:NP820706.RAzd4EkGxapVel7UgOK8I50pPtCoDxOSgKNIWeeEZyVXQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP820706.RAzd4EkGxapVel7UgOK8I50pPtCoDxOSgKNIWeeEZyVXQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP820706.RAzd4EkGxapVel7UgOK8I50pPtCoDxOSgKNIWeeEZyVXQ130_assertion a np:Assertion .
  dgn-np:NP820706.RAzd4EkGxapVel7UgOK8I50pPtCoDxOSgKNIWeeEZyVXQ130_provenance a np:Provenance .
  dgn-np:NP820706.RAzd4EkGxapVel7UgOK8I50pPtCoDxOSgKNIWeeEZyVXQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP820706.RAzd4EkGxapVel7UgOK8I50pPtCoDxOSgKNIWeeEZyVXQ130_assertion {
  miriam-gene:9360 a ncit:C16612 .
  lld:C0006142 a ncit:C7057 .
  dgn-gda:DGN13d4c3ff09d012fe4875d13b7f2d5bb6 sio:SIO_000628 miriam-gene:9360 , lld:C0006142 ;
    a sio:SIO_001122 .
}
dgn-np:NP820706.RAzd4EkGxapVel7UgOK8I50pPtCoDxOSgKNIWeeEZyVXQ130_provenance {
  dgn-np:NP820706.RAzd4EkGxapVel7UgOK8I50pPtCoDxOSgKNIWeeEZyVXQ130_assertion dcterms:description "[Among other genetic markers, thrombophilic genetic variants, such as the Factor V Leiden and prothrombin G20210A polymorphisms, as well as genetic variants of cytochrome P450 (CYP) enzymes, for example, CYP19 and CYP1B1, have been established as genetic risk markers and disease modifiers of recurrent and sporadic pregnancy loss and HRT-independent and -dependent breast cancer, respectively.]. 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:14683420 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP820706.RAzd4EkGxapVel7UgOK8I50pPtCoDxOSgKNIWeeEZyVXQ130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:57+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" .
}