@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP282088.RAlxRMdSTyTw8i_g2Fz21lSoVYplw_NepYohOmrHNdT1A> .
@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:NP282088.RAlxRMdSTyTw8i_g2Fz21lSoVYplw_NepYohOmrHNdT1A130_head {
  this: np:hasAssertion dgn-np:NP282088.RAlxRMdSTyTw8i_g2Fz21lSoVYplw_NepYohOmrHNdT1A130_assertion;
    np:hasProvenance dgn-np:NP282088.RAlxRMdSTyTw8i_g2Fz21lSoVYplw_NepYohOmrHNdT1A130_provenance;
    np:hasPublicationInfo dgn-np:NP282088.RAlxRMdSTyTw8i_g2Fz21lSoVYplw_NepYohOmrHNdT1A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP282088.RAlxRMdSTyTw8i_g2Fz21lSoVYplw_NepYohOmrHNdT1A130_assertion a np:Assertion .
  
  dgn-np:NP282088.RAlxRMdSTyTw8i_g2Fz21lSoVYplw_NepYohOmrHNdT1A130_provenance a np:Provenance .
  
  dgn-np:NP282088.RAlxRMdSTyTw8i_g2Fz21lSoVYplw_NepYohOmrHNdT1A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP282088.RAlxRMdSTyTw8i_g2Fz21lSoVYplw_NepYohOmrHNdT1A130_assertion {
  miriam-gene:338 a ncit:C16612 .
  
  lld:C0948008 a ncit:C7057 .
  
  dgn-gda:DGN5ee9c230e1a268c2ca8bcc880a140c31 sio:SIO_000628 miriam-gene:338, lld:C0948008;
    a sio:SIO_001121 .
}

dgn-np:NP282088.RAlxRMdSTyTw8i_g2Fz21lSoVYplw_NepYohOmrHNdT1A130_provenance {
  dgn-np:NP282088.RAlxRMdSTyTw8i_g2Fz21lSoVYplw_NepYohOmrHNdT1A130_assertion dcterms:description
      "[We tested the hypothesis that the APOB T71I, A591V, P2712L, R3611Q, E4154K, and N4311S polymorphisms associate with risk of ischemic stroke in the general population and performed in vivo human LDL turnover studies of E4154K heterozygotes vs. K4154K homozygotes.]. 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:17595251;
    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:NP282088.RAlxRMdSTyTw8i_g2Fz21lSoVYplw_NepYohOmrHNdT1A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:39+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" .
}