@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP757094.RAtTbtk9UT-wSTrUTFp0nlhUrBPl7PoXysaB_w_yF5-Cw> .
@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:NP757094.RAtTbtk9UT-wSTrUTFp0nlhUrBPl7PoXysaB_w_yF5-Cw130_head {
  this: np:hasAssertion dgn-np:NP757094.RAtTbtk9UT-wSTrUTFp0nlhUrBPl7PoXysaB_w_yF5-Cw130_assertion ;
    np:hasProvenance dgn-np:NP757094.RAtTbtk9UT-wSTrUTFp0nlhUrBPl7PoXysaB_w_yF5-Cw130_provenance ;
    np:hasPublicationInfo dgn-np:NP757094.RAtTbtk9UT-wSTrUTFp0nlhUrBPl7PoXysaB_w_yF5-Cw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP757094.RAtTbtk9UT-wSTrUTFp0nlhUrBPl7PoXysaB_w_yF5-Cw130_assertion a np:Assertion .
  dgn-np:NP757094.RAtTbtk9UT-wSTrUTFp0nlhUrBPl7PoXysaB_w_yF5-Cw130_provenance a np:Provenance .
  dgn-np:NP757094.RAtTbtk9UT-wSTrUTFp0nlhUrBPl7PoXysaB_w_yF5-Cw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP757094.RAtTbtk9UT-wSTrUTFp0nlhUrBPl7PoXysaB_w_yF5-Cw130_assertion {
  miriam-gene:10205 a ncit:C16612 .
  lld:C0004153 a ncit:C7057 .
  dgn-gda:DGNe05ddcf09cebff6458ab9f4bb28293db sio:SIO_000628 miriam-gene:10205 , lld:C0004153 ;
    a sio:SIO_001121 .
}
dgn-np:NP757094.RAtTbtk9UT-wSTrUTFp0nlhUrBPl7PoXysaB_w_yF5-Cw130_provenance {
  dgn-np:NP757094.RAtTbtk9UT-wSTrUTFp0nlhUrBPl7PoXysaB_w_yF5-Cw130_assertion dcterms:description "[To check its possible implication in atherosclerosis, this polymorphism was then genotyped in the AXA Study (ultrasound examinations of carotid and femoral arteries in the context of an employment medical examination, 733 subjects), the EVA Study (ultrasound examinations of carotid arteries in a study of cognitive and vascular ageing, 1092 subjects) and the GENIC Study (on brain infarction (BI), 912 subjects).]. 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:14694358 ;
    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:NP757094.RAtTbtk9UT-wSTrUTFp0nlhUrBPl7PoXysaB_w_yF5-Cw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:38+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" .
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}