@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP63260.RAYvrL9MeKSqjLrZ7kUJYDPWu2KACNvmN4BCpVMoUNLd0> .
@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:NP63260.RAYvrL9MeKSqjLrZ7kUJYDPWu2KACNvmN4BCpVMoUNLd0130_head {
  this: np:hasAssertion dgn-np:NP63260.RAYvrL9MeKSqjLrZ7kUJYDPWu2KACNvmN4BCpVMoUNLd0130_assertion;
    np:hasProvenance dgn-np:NP63260.RAYvrL9MeKSqjLrZ7kUJYDPWu2KACNvmN4BCpVMoUNLd0130_provenance;
    np:hasPublicationInfo dgn-np:NP63260.RAYvrL9MeKSqjLrZ7kUJYDPWu2KACNvmN4BCpVMoUNLd0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP63260.RAYvrL9MeKSqjLrZ7kUJYDPWu2KACNvmN4BCpVMoUNLd0130_assertion a np:Assertion .
  
  dgn-np:NP63260.RAYvrL9MeKSqjLrZ7kUJYDPWu2KACNvmN4BCpVMoUNLd0130_provenance a np:Provenance .
  
  dgn-np:NP63260.RAYvrL9MeKSqjLrZ7kUJYDPWu2KACNvmN4BCpVMoUNLd0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP63260.RAYvrL9MeKSqjLrZ7kUJYDPWu2KACNvmN4BCpVMoUNLd0130_assertion {
  miriam-gene:3690 a ncit:C16612 .
  
  lld:C0038525 a ncit:C7057 .
  
  dgn-gda:DGN6be50f89f8e157601f36c28f868d308b sio:SIO_000628 miriam-gene:3690, lld:C0038525;
    a sio:SIO_001122 .
}

dgn-np:NP63260.RAYvrL9MeKSqjLrZ7kUJYDPWu2KACNvmN4BCpVMoUNLd0130_provenance {
  dgn-np:NP63260.RAYvrL9MeKSqjLrZ7kUJYDPWu2KACNvmN4BCpVMoUNLd0130_assertion dcterms:description
      "[ We present the first evidence suggesting a protective role for the platelet GPIIIa HPA-1b allele in SAH. The suggested platelet hyper-reactivity determined by this allele could reduce the risk to suffer SAH, specially if the aneurysm is small, attenuate the severity of the hemorrhage, and reduce the clinical grade at presentation. This effect might be amplified by the simultaneous combination with the GPIbalpha HPA-2b allele.]. 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:15331787;
    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:NP63260.RAYvrL9MeKSqjLrZ7kUJYDPWu2KACNvmN4BCpVMoUNLd0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:30+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" .
}