@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP257827.RAEmTsHYgV2kw-VvjClV93KwFqxe5qoAVAeo5mxFKvQ38> .
@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:NP257827.RAEmTsHYgV2kw-VvjClV93KwFqxe5qoAVAeo5mxFKvQ38130_head {
  this: np:hasAssertion dgn-np:NP257827.RAEmTsHYgV2kw-VvjClV93KwFqxe5qoAVAeo5mxFKvQ38130_assertion ;
    np:hasProvenance dgn-np:NP257827.RAEmTsHYgV2kw-VvjClV93KwFqxe5qoAVAeo5mxFKvQ38130_provenance ;
    np:hasPublicationInfo dgn-np:NP257827.RAEmTsHYgV2kw-VvjClV93KwFqxe5qoAVAeo5mxFKvQ38130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP257827.RAEmTsHYgV2kw-VvjClV93KwFqxe5qoAVAeo5mxFKvQ38130_assertion a np:Assertion .
  dgn-np:NP257827.RAEmTsHYgV2kw-VvjClV93KwFqxe5qoAVAeo5mxFKvQ38130_provenance a np:Provenance .
  dgn-np:NP257827.RAEmTsHYgV2kw-VvjClV93KwFqxe5qoAVAeo5mxFKvQ38130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP257827.RAEmTsHYgV2kw-VvjClV93KwFqxe5qoAVAeo5mxFKvQ38130_assertion {
  miriam-gene:2157 a ncit:C16612 .
  lld:C0584960 a ncit:C7057 .
  dgn-gda:DGNa61a0a100901fc972a9118bc6ccd9104 sio:SIO_000628 miriam-gene:2157 , lld:C0584960 ;
    a sio:SIO_001121 .
}
dgn-np:NP257827.RAEmTsHYgV2kw-VvjClV93KwFqxe5qoAVAeo5mxFKvQ38130_provenance {
  dgn-np:NP257827.RAEmTsHYgV2kw-VvjClV93KwFqxe5qoAVAeo5mxFKvQ38130_assertion dcterms:description "[To determine whether the factor V Leiden mutation is associated with decreased bleeding in individuals with severe hemophilia A, factor concentrate utilization, maximum annual number of bleeding episodes, and the prevalence of hemophilic arthropathy between carriers and non-carriers of the factor V Leiden mutation were compared.]. 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:10744141 ;
    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:NP257827.RAEmTsHYgV2kw-VvjClV93KwFqxe5qoAVAeo5mxFKvQ38130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:24+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" .
}