@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP278156.RAHbGT4TKaqYnhBBNn_WHSxalwq4okvxi3gnktYjU1Oh8> .
@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:NP278156.RAHbGT4TKaqYnhBBNn_WHSxalwq4okvxi3gnktYjU1Oh8130_head {
  this: np:hasAssertion dgn-np:NP278156.RAHbGT4TKaqYnhBBNn_WHSxalwq4okvxi3gnktYjU1Oh8130_assertion;
    np:hasProvenance dgn-np:NP278156.RAHbGT4TKaqYnhBBNn_WHSxalwq4okvxi3gnktYjU1Oh8130_provenance;
    np:hasPublicationInfo dgn-np:NP278156.RAHbGT4TKaqYnhBBNn_WHSxalwq4okvxi3gnktYjU1Oh8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP278156.RAHbGT4TKaqYnhBBNn_WHSxalwq4okvxi3gnktYjU1Oh8130_assertion a np:Assertion .
  
  dgn-np:NP278156.RAHbGT4TKaqYnhBBNn_WHSxalwq4okvxi3gnktYjU1Oh8130_provenance a np:Provenance .
  
  dgn-np:NP278156.RAHbGT4TKaqYnhBBNn_WHSxalwq4okvxi3gnktYjU1Oh8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP278156.RAHbGT4TKaqYnhBBNn_WHSxalwq4okvxi3gnktYjU1Oh8130_assertion {
  miriam-gene:4233 a ncit:C16612 .
  
  lld:C0010674 a ncit:C7057 .
  
  dgn-gda:DGN08261ddef4ac53873763c25fe73e7e3a sio:SIO_000628 miriam-gene:4233, lld:C0010674;
    a sio:SIO_001121 .
}

dgn-np:NP278156.RAHbGT4TKaqYnhBBNn_WHSxalwq4okvxi3gnktYjU1Oh8130_provenance {
  dgn-np:NP278156.RAHbGT4TKaqYnhBBNn_WHSxalwq4okvxi3gnktYjU1Oh8130_assertion dcterms:description
      "[In family studies using this polymorphism, genetic linkage was found between PAI1 and the loci for erythropoietin (EPO), paraoxonase (PON), the met protooncogene (MET), and cystic fibrosis (CF), all previously assigned to the middle part of the long arm of chromosome 7.]. 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:2891140;
    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:NP278156.RAHbGT4TKaqYnhBBNn_WHSxalwq4okvxi3gnktYjU1Oh8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:37+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" .
}