@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1362443.RAtyUCqw3tIPyF8rhnAFFwGmQNvZ6siQMeAb2K3DglW8Y> .
@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:NP1362443.RAtyUCqw3tIPyF8rhnAFFwGmQNvZ6siQMeAb2K3DglW8Y130_head {
  this: np:hasAssertion dgn-np:NP1362443.RAtyUCqw3tIPyF8rhnAFFwGmQNvZ6siQMeAb2K3DglW8Y130_assertion;
    np:hasProvenance dgn-np:NP1362443.RAtyUCqw3tIPyF8rhnAFFwGmQNvZ6siQMeAb2K3DglW8Y130_provenance;
    np:hasPublicationInfo dgn-np:NP1362443.RAtyUCqw3tIPyF8rhnAFFwGmQNvZ6siQMeAb2K3DglW8Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1362443.RAtyUCqw3tIPyF8rhnAFFwGmQNvZ6siQMeAb2K3DglW8Y130_assertion a np:Assertion .
  
  dgn-np:NP1362443.RAtyUCqw3tIPyF8rhnAFFwGmQNvZ6siQMeAb2K3DglW8Y130_provenance a np:Provenance .
  
  dgn-np:NP1362443.RAtyUCqw3tIPyF8rhnAFFwGmQNvZ6siQMeAb2K3DglW8Y130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1362443.RAtyUCqw3tIPyF8rhnAFFwGmQNvZ6siQMeAb2K3DglW8Y130_assertion {
  miriam-gene:3674 a ncit:C16612 .
  
  lld:C0005129 a ncit:C7057 .
  
  dgn-gda:DGN01d37bcceab462114ffb0b0771fadca7 sio:SIO_000628 miriam-gene:3674, lld:C0005129;
    a sio:SIO_001121 .
}

dgn-np:NP1362443.RAtyUCqw3tIPyF8rhnAFFwGmQNvZ6siQMeAb2K3DglW8Y130_provenance {
  dgn-np:NP1362443.RAtyUCqw3tIPyF8rhnAFFwGmQNvZ6siQMeAb2K3DglW8Y130_assertion dcterms:description
      "[While encountered only rarely, carriers of either GT or Bernard Soulier syndrome that are at the same time heterozygous for human platelet alloantigenic epitopes found on GPIb, GPIIb, or GPIIIa have the possibility to give discrepant results when comparing genotypic versus phenotypic analysis.]. 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:8916947;
    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:NP1362443.RAtyUCqw3tIPyF8rhnAFFwGmQNvZ6siQMeAb2K3DglW8Y130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:03+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" .
}