@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP49607.RAvJmUzpz8dcgjBkJN2q6o4rYu14C0TlcZXnDP-Ct5OIw> .
@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:NP49607.RAvJmUzpz8dcgjBkJN2q6o4rYu14C0TlcZXnDP-Ct5OIw130_head {
  this: np:hasAssertion dgn-np:NP49607.RAvJmUzpz8dcgjBkJN2q6o4rYu14C0TlcZXnDP-Ct5OIw130_assertion;
    np:hasProvenance dgn-np:NP49607.RAvJmUzpz8dcgjBkJN2q6o4rYu14C0TlcZXnDP-Ct5OIw130_provenance;
    np:hasPublicationInfo dgn-np:NP49607.RAvJmUzpz8dcgjBkJN2q6o4rYu14C0TlcZXnDP-Ct5OIw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP49607.RAvJmUzpz8dcgjBkJN2q6o4rYu14C0TlcZXnDP-Ct5OIw130_assertion a np:Assertion .
  
  dgn-np:NP49607.RAvJmUzpz8dcgjBkJN2q6o4rYu14C0TlcZXnDP-Ct5OIw130_provenance a np:Provenance .
  
  dgn-np:NP49607.RAvJmUzpz8dcgjBkJN2q6o4rYu14C0TlcZXnDP-Ct5OIw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP49607.RAvJmUzpz8dcgjBkJN2q6o4rYu14C0TlcZXnDP-Ct5OIw130_assertion {
  miriam-gene:1636 a ncit:C16612 .
  
  lld:C0948163 a ncit:C7057 .
  
  dgn-gda:DGN0789261edfec83d1f5344bc5e2ee5b06 sio:SIO_000628 miriam-gene:1636, lld:C0948163;
    a sio:SIO_001122 .
}

dgn-np:NP49607.RAvJmUzpz8dcgjBkJN2q6o4rYu14C0TlcZXnDP-Ct5OIw130_provenance {
  dgn-np:NP49607.RAvJmUzpz8dcgjBkJN2q6o4rYu14C0TlcZXnDP-Ct5OIw130_assertion dcterms:description
      "[ This study supports the hypothesis that there may be different types of small vessel disease in patients with classic lacunar syndromes and that the influence of the ACE DD genotype may be relevant in mediating the diffuse form of vessel injury.]. 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:11861692;
    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:NP49607.RAvJmUzpz8dcgjBkJN2q6o4rYu14C0TlcZXnDP-Ct5OIw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:23+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" .
}