@prefix dct: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP936035.RAL3A5EEatCkMUrhRxEk1pUC1eKp3qejlqh7Q89NYGYbc> .
@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 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:NP936035.RAL3A5EEatCkMUrhRxEk1pUC1eKp3qejlqh7Q89NYGYbc130_head {
  this: np:hasAssertion dgn-np:NP936035.RAL3A5EEatCkMUrhRxEk1pUC1eKp3qejlqh7Q89NYGYbc130_assertion;
    np:hasProvenance dgn-np:NP936035.RAL3A5EEatCkMUrhRxEk1pUC1eKp3qejlqh7Q89NYGYbc130_provenance;
    np:hasPublicationInfo dgn-np:NP936035.RAL3A5EEatCkMUrhRxEk1pUC1eKp3qejlqh7Q89NYGYbc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP936035.RAL3A5EEatCkMUrhRxEk1pUC1eKp3qejlqh7Q89NYGYbc130_assertion a np:Assertion .
  
  dgn-np:NP936035.RAL3A5EEatCkMUrhRxEk1pUC1eKp3qejlqh7Q89NYGYbc130_provenance a np:Provenance .
  
  dgn-np:NP936035.RAL3A5EEatCkMUrhRxEk1pUC1eKp3qejlqh7Q89NYGYbc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP936035.RAL3A5EEatCkMUrhRxEk1pUC1eKp3qejlqh7Q89NYGYbc130_assertion {
  miriam-gene:9370 a ncit:C16612 .
  
  lld:C1859727 a ncit:C7057 .
  
  dgn-gda:DGN037c7bfa44e0c51e8c3541077ed98c62 sio:SIO_000628 miriam-gene:9370, lld:C1859727;
    a sio:SIO_001121 .
}

dgn-np:NP936035.RAL3A5EEatCkMUrhRxEk1pUC1eKp3qejlqh7Q89NYGYbc130_provenance {
  dgn-np:NP936035.RAL3A5EEatCkMUrhRxEk1pUC1eKp3qejlqh7Q89NYGYbc130_assertion dct:description
      "[Monogenic ENPP1, CD73, and ABCC6 deficiencies each drive a molecular pathophysiology of closely related but phenotypically different diseases (generalized arterial calcification of infancy (GACI), pseudoxanthoma elasticum (PXE) and arterial calcification caused by CD73 deficiency (ACDC)), in which premature onset arterial calcification is a prominent but not the sole feature.]. 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:21852556;
    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:NP936035.RAL3A5EEatCkMUrhRxEk1pUC1eKp3qejlqh7Q89NYGYbc130_publicationInfo {
  this: dct:created "2014-10-02T12:41:33+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct: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" .
}