@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP77795.RASCzdVjJDtZ-CBZzsCGNfBXdRZvLxxWs_V88aP30X4Xc> .
@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:NP77795.RASCzdVjJDtZ-CBZzsCGNfBXdRZvLxxWs_V88aP30X4Xc130_head {
  this: np:hasAssertion dgn-np:NP77795.RASCzdVjJDtZ-CBZzsCGNfBXdRZvLxxWs_V88aP30X4Xc130_assertion;
    np:hasProvenance dgn-np:NP77795.RASCzdVjJDtZ-CBZzsCGNfBXdRZvLxxWs_V88aP30X4Xc130_provenance;
    np:hasPublicationInfo dgn-np:NP77795.RASCzdVjJDtZ-CBZzsCGNfBXdRZvLxxWs_V88aP30X4Xc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP77795.RASCzdVjJDtZ-CBZzsCGNfBXdRZvLxxWs_V88aP30X4Xc130_assertion a np:Assertion .
  
  dgn-np:NP77795.RASCzdVjJDtZ-CBZzsCGNfBXdRZvLxxWs_V88aP30X4Xc130_provenance a np:Provenance .
  
  dgn-np:NP77795.RASCzdVjJDtZ-CBZzsCGNfBXdRZvLxxWs_V88aP30X4Xc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP77795.RASCzdVjJDtZ-CBZzsCGNfBXdRZvLxxWs_V88aP30X4Xc130_assertion {
  miriam-gene:1136 a ncit:C16612 .
  
  lld:C0085096 a ncit:C7057 .
  
  dgn-gda:DGNca605e5e4fdb6ae266e46d8c4ca7becb sio:SIO_000628 miriam-gene:1136, lld:C0085096;
    a sio:SIO_001122 .
}

dgn-np:NP77795.RASCzdVjJDtZ-CBZzsCGNfBXdRZvLxxWs_V88aP30X4Xc130_provenance {
  dgn-np:NP77795.RASCzdVjJDtZ-CBZzsCGNfBXdRZvLxxWs_V88aP30X4Xc130_assertion dcterms:description
      "[Twenty-three polymorphisms in 22 potential PAD candidate genes (F2, FGB, MTHFR, ITGB3, ACE, AGT, IL6, CCL2, ICAM1, SELE, MMP9, PPARG, MMP1, ADD1, P2RY12, LIPC, PLA2G7, SCARB1, MMP3, MTTP, LPA, CHRNA3) showed a significant association in individual studies.]. 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:19435865;
    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:NP77795.RASCzdVjJDtZ-CBZzsCGNfBXdRZvLxxWs_V88aP30X4Xc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:38+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" .
}