@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP920293.RAQTfr_JGyas41IYc7NF_V4foUkVDG220UfvnXgEXbP54> .
@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:NP920293.RAQTfr_JGyas41IYc7NF_V4foUkVDG220UfvnXgEXbP54130_head {
  this: np:hasAssertion dgn-np:NP920293.RAQTfr_JGyas41IYc7NF_V4foUkVDG220UfvnXgEXbP54130_assertion ;
    np:hasProvenance dgn-np:NP920293.RAQTfr_JGyas41IYc7NF_V4foUkVDG220UfvnXgEXbP54130_provenance ;
    np:hasPublicationInfo dgn-np:NP920293.RAQTfr_JGyas41IYc7NF_V4foUkVDG220UfvnXgEXbP54130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP920293.RAQTfr_JGyas41IYc7NF_V4foUkVDG220UfvnXgEXbP54130_assertion a np:Assertion .
  dgn-np:NP920293.RAQTfr_JGyas41IYc7NF_V4foUkVDG220UfvnXgEXbP54130_provenance a np:Provenance .
  dgn-np:NP920293.RAQTfr_JGyas41IYc7NF_V4foUkVDG220UfvnXgEXbP54130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP920293.RAQTfr_JGyas41IYc7NF_V4foUkVDG220UfvnXgEXbP54130_assertion {
  miriam-gene:7450 a ncit:C16612 .
  lld:C0010054 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP920293.RAQTfr_JGyas41IYc7NF_V4foUkVDG220UfvnXgEXbP54130_provenance {
  dgn-np:NP920293.RAQTfr_JGyas41IYc7NF_V4foUkVDG220UfvnXgEXbP54130_assertion dcterms:description "[We describe a significant proportion of individual TS females having high levels of vWF, factor VIII, fibrinogen and CRP (15-40%) and an increased frequency of the Leiden mutation, with important associations with CIMT and blood pressure, suggesting that a subset of TS may have an unfavourable haemostatic balance, which may contribute to the increased risk of premature ischaemic heart disease and possibly increase the risk of deep venous and portal vein thrombosis.]. 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:21848660 ;
    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 .
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dgn-np:NP920293.RAQTfr_JGyas41IYc7NF_V4foUkVDG220UfvnXgEXbP54130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:24+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> ;
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}