@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP323900.RAsAyaY5fKHx6xTAeqYwHH58PiQqMss52j_HYwzHGmAnU> .
@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:NP323900.RAsAyaY5fKHx6xTAeqYwHH58PiQqMss52j_HYwzHGmAnU130_head {
  this: np:hasAssertion dgn-np:NP323900.RAsAyaY5fKHx6xTAeqYwHH58PiQqMss52j_HYwzHGmAnU130_assertion;
    np:hasProvenance dgn-np:NP323900.RAsAyaY5fKHx6xTAeqYwHH58PiQqMss52j_HYwzHGmAnU130_provenance;
    np:hasPublicationInfo dgn-np:NP323900.RAsAyaY5fKHx6xTAeqYwHH58PiQqMss52j_HYwzHGmAnU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP323900.RAsAyaY5fKHx6xTAeqYwHH58PiQqMss52j_HYwzHGmAnU130_assertion a np:Assertion .
  
  dgn-np:NP323900.RAsAyaY5fKHx6xTAeqYwHH58PiQqMss52j_HYwzHGmAnU130_provenance a np:Provenance .
  
  dgn-np:NP323900.RAsAyaY5fKHx6xTAeqYwHH58PiQqMss52j_HYwzHGmAnU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP323900.RAsAyaY5fKHx6xTAeqYwHH58PiQqMss52j_HYwzHGmAnU130_assertion {
  miriam-gene:84159 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
  dgn-gda:DGN0becad0bea63e44e858cad357e3e5b3a sio:SIO_000628 miriam-gene:84159, lld:C0011860;
    a sio:SIO_001121 .
}

dgn-np:NP323900.RAsAyaY5fKHx6xTAeqYwHH58PiQqMss52j_HYwzHGmAnU130_provenance {
  dgn-np:NP323900.RAsAyaY5fKHx6xTAeqYwHH58PiQqMss52j_HYwzHGmAnU130_assertion dcterms:description
      "[The study was aimed to determine whether any of the four MRF2/ARID5B SNPs (rs2893880, rs10740055, rs7087507 and rs10761600) associated with susceptibility to CAD are also associated with T2D, and to determine whether SNP genotype influences the levels of adiponectin and other clinical factors.]. 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:22971728;
    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:NP323900.RAsAyaY5fKHx6xTAeqYwHH58PiQqMss52j_HYwzHGmAnU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:09+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" .
}