@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48461.RAv-EEMxKTivT6SA7n3vOkgibUlXx-_DEfuID5nPJR77A> .
@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 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:NP48461.RAv-EEMxKTivT6SA7n3vOkgibUlXx-_DEfuID5nPJR77A130_head {
  this: np:hasAssertion dgn-np:NP48461.RAv-EEMxKTivT6SA7n3vOkgibUlXx-_DEfuID5nPJR77A130_assertion ;
    np:hasProvenance dgn-np:NP48461.RAv-EEMxKTivT6SA7n3vOkgibUlXx-_DEfuID5nPJR77A130_provenance ;
    np:hasPublicationInfo dgn-np:NP48461.RAv-EEMxKTivT6SA7n3vOkgibUlXx-_DEfuID5nPJR77A130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP48461.RAv-EEMxKTivT6SA7n3vOkgibUlXx-_DEfuID5nPJR77A130_assertion a np:Assertion .
  dgn-np:NP48461.RAv-EEMxKTivT6SA7n3vOkgibUlXx-_DEfuID5nPJR77A130_provenance a np:Provenance .
  dgn-np:NP48461.RAv-EEMxKTivT6SA7n3vOkgibUlXx-_DEfuID5nPJR77A130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP48461.RAv-EEMxKTivT6SA7n3vOkgibUlXx-_DEfuID5nPJR77A130_assertion {
  miriam-gene:335 a ncit:C16612 .
  lld:C1956346 a ncit:C7057 .
  dgn-gda:DGNd1852d880875c1b576c16d42a309b45b sio:SIO_000628 miriam-gene:335 , lld:C1956346 ;
    a sio:SIO_001122 .
}
dgn-np:NP48461.RAv-EEMxKTivT6SA7n3vOkgibUlXx-_DEfuID5nPJR77A130_provenance {
  dgn-np:NP48461.RAv-EEMxKTivT6SA7n3vOkgibUlXx-_DEfuID5nPJR77A130_assertion dct:description "[Both approaches (association analysis and gametic disequilibrium) revealed the same gene combinations contributing to the CAD risk factors. NOS3 and APOA1 markers were in gametic disequilibrium in the patients and both of them were associated with LDL. F13 and AGT were associated with systolic and diastolic blood pressure and two-locus gametic disequilibrium between F13 and AGT polymorphisms observed in the patients.]. 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:11507973 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP48461.RAv-EEMxKTivT6SA7n3vOkgibUlXx-_DEfuID5nPJR77A130_publicationInfo {
  this: dct:created "2014-10-02T12:32:22+02:00"^^xsd:dateTime ;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dct:rightsHolder dgn-void:IBIGroup ;
    dct:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}