@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP50492.RAsjTyxe4HaQtYQriBCxeJfAZzW6RP5621JoMHN0oB6VY> .
@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:NP50492.RAsjTyxe4HaQtYQriBCxeJfAZzW6RP5621JoMHN0oB6VY130_head {
  this: np:hasAssertion dgn-np:NP50492.RAsjTyxe4HaQtYQriBCxeJfAZzW6RP5621JoMHN0oB6VY130_assertion;
    np:hasProvenance dgn-np:NP50492.RAsjTyxe4HaQtYQriBCxeJfAZzW6RP5621JoMHN0oB6VY130_provenance;
    np:hasPublicationInfo dgn-np:NP50492.RAsjTyxe4HaQtYQriBCxeJfAZzW6RP5621JoMHN0oB6VY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP50492.RAsjTyxe4HaQtYQriBCxeJfAZzW6RP5621JoMHN0oB6VY130_assertion a np:Assertion .
  
  dgn-np:NP50492.RAsjTyxe4HaQtYQriBCxeJfAZzW6RP5621JoMHN0oB6VY130_provenance a np:Provenance .
  
  dgn-np:NP50492.RAsjTyxe4HaQtYQriBCxeJfAZzW6RP5621JoMHN0oB6VY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP50492.RAsjTyxe4HaQtYQriBCxeJfAZzW6RP5621JoMHN0oB6VY130_assertion {
  miriam-gene:7060 a ncit:C16612 .
  
  lld:C0027051 a ncit:C7057 .
  
  dgn-gda:DGN9ed72b4a71da658bdf22f656ecc5b04e sio:SIO_000628 miriam-gene:7060, lld:C0027051;
    a sio:SIO_001122 .
}

dgn-np:NP50492.RAsjTyxe4HaQtYQriBCxeJfAZzW6RP5621JoMHN0oB6VY130_provenance {
  dgn-np:NP50492.RAsjTyxe4HaQtYQriBCxeJfAZzW6RP5621JoMHN0oB6VY130_assertion dcterms:description
      "[ Our findings suggest that the A387P variant of the THBS4 gene may be an important determinant in the development of MI at any age. Careful assessment of clinical covariates helped to unmask a significant association and therefore may be an important reason for why studies do not replicate.]. 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:15131549;
    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:NP50492.RAsjTyxe4HaQtYQriBCxeJfAZzW6RP5621JoMHN0oB6VY130_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" .
}