@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59006.RA6n4tOXHA1gfVNzzijPuAMckadcpTWwvI3p2VZcbRJoY> .
@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:NP59006.RA6n4tOXHA1gfVNzzijPuAMckadcpTWwvI3p2VZcbRJoY130_head {
  this: np:hasAssertion dgn-np:NP59006.RA6n4tOXHA1gfVNzzijPuAMckadcpTWwvI3p2VZcbRJoY130_assertion;
    np:hasProvenance dgn-np:NP59006.RA6n4tOXHA1gfVNzzijPuAMckadcpTWwvI3p2VZcbRJoY130_provenance;
    np:hasPublicationInfo dgn-np:NP59006.RA6n4tOXHA1gfVNzzijPuAMckadcpTWwvI3p2VZcbRJoY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP59006.RA6n4tOXHA1gfVNzzijPuAMckadcpTWwvI3p2VZcbRJoY130_assertion a np:Assertion .
  
  dgn-np:NP59006.RA6n4tOXHA1gfVNzzijPuAMckadcpTWwvI3p2VZcbRJoY130_provenance a np:Provenance .
  
  dgn-np:NP59006.RA6n4tOXHA1gfVNzzijPuAMckadcpTWwvI3p2VZcbRJoY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP59006.RA6n4tOXHA1gfVNzzijPuAMckadcpTWwvI3p2VZcbRJoY130_assertion {
  miriam-gene:7421 a ncit:C16612 .
  
  lld:C0026769 a ncit:C7057 .
  
  dgn-gda:DGN401e1784d3c3b9d613bb8876560b8dc9 sio:SIO_000628 miriam-gene:7421, lld:C0026769;
    a sio:SIO_001122 .
}

dgn-np:NP59006.RA6n4tOXHA1gfVNzzijPuAMckadcpTWwvI3p2VZcbRJoY130_provenance {
  dgn-np:NP59006.RA6n4tOXHA1gfVNzzijPuAMckadcpTWwvI3p2VZcbRJoY130_assertion dct:description
      "[The results indicate for the first time an association of MS with VDRG polymorphism, which may be involved in pathogenesis of MS, or in the linkage disequilibrium of VDRG to another pathogenic gene loci. ]. 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:10465499;
    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:NP59006.RA6n4tOXHA1gfVNzzijPuAMckadcpTWwvI3p2VZcbRJoY130_publicationInfo {
  this: dct:created "2014-10-02T12:32:27+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 orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}