@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP850975.RAibPPieh1iYPlpLbXnumiQV859yE5kLlh0_ihO3KD-7E> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP850975.RAibPPieh1iYPlpLbXnumiQV859yE5kLlh0_ihO3KD-7E130_head {
  this: np:hasAssertion dgn-np:NP850975.RAibPPieh1iYPlpLbXnumiQV859yE5kLlh0_ihO3KD-7E130_assertion;
    np:hasProvenance dgn-np:NP850975.RAibPPieh1iYPlpLbXnumiQV859yE5kLlh0_ihO3KD-7E130_provenance;
    np:hasPublicationInfo dgn-np:NP850975.RAibPPieh1iYPlpLbXnumiQV859yE5kLlh0_ihO3KD-7E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP850975.RAibPPieh1iYPlpLbXnumiQV859yE5kLlh0_ihO3KD-7E130_assertion a np:Assertion .
  
  dgn-np:NP850975.RAibPPieh1iYPlpLbXnumiQV859yE5kLlh0_ihO3KD-7E130_provenance a np:Provenance .
  
  dgn-np:NP850975.RAibPPieh1iYPlpLbXnumiQV859yE5kLlh0_ihO3KD-7E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP850975.RAibPPieh1iYPlpLbXnumiQV859yE5kLlh0_ihO3KD-7E130_assertion {
  miriam-gene:4854 a ncit:C16612 .
  
  lld:C0038454 a ncit:C7057 .
  
  dgn-gda:DGNaed32bbce08dd6ce075cac8cd9416db5 sio:SIO_000628 miriam-gene:4854, lld:C0038454;
    a sio:SIO_001121 .
}

dgn-np:NP850975.RAibPPieh1iYPlpLbXnumiQV859yE5kLlh0_ihO3KD-7E130_provenance {
  dgn-np:NP850975.RAibPPieh1iYPlpLbXnumiQV859yE5kLlh0_ihO3KD-7E130_assertion dcterms:description
      "[Also reviewed is recent progress in understanding single-gene disorders in which stroke is a major feature of the phenotype, including CADASIL, CARASIL, hereditary angiopathy with nephropathy, aneurysm and muscle cramps, and Fabry disease and progress in pharmacogenomics as it relates to response to antiplatelet therapy.]. 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:21058051;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP850975.RAibPPieh1iYPlpLbXnumiQV859yE5kLlh0_ihO3KD-7E130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:10+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}