@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP696108.RAX3gWURgWCspjYhLiHj22gxL45e5ITfPgAQUAjDLRsXw> .
@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:NP696108.RAX3gWURgWCspjYhLiHj22gxL45e5ITfPgAQUAjDLRsXw130_head {
  this: np:hasAssertion dgn-np:NP696108.RAX3gWURgWCspjYhLiHj22gxL45e5ITfPgAQUAjDLRsXw130_assertion;
    np:hasProvenance dgn-np:NP696108.RAX3gWURgWCspjYhLiHj22gxL45e5ITfPgAQUAjDLRsXw130_provenance;
    np:hasPublicationInfo dgn-np:NP696108.RAX3gWURgWCspjYhLiHj22gxL45e5ITfPgAQUAjDLRsXw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP696108.RAX3gWURgWCspjYhLiHj22gxL45e5ITfPgAQUAjDLRsXw130_assertion a np:Assertion .
  
  dgn-np:NP696108.RAX3gWURgWCspjYhLiHj22gxL45e5ITfPgAQUAjDLRsXw130_provenance a np:Provenance .
  
  dgn-np:NP696108.RAX3gWURgWCspjYhLiHj22gxL45e5ITfPgAQUAjDLRsXw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP696108.RAX3gWURgWCspjYhLiHj22gxL45e5ITfPgAQUAjDLRsXw130_assertion {
  miriam-gene:368 a ncit:C16612 .
  
  lld:C0035435 a ncit:C7057 .
  
  dgn-gda:DGN279954950e35331346e1ff64e16188a7 sio:SIO_000628 miriam-gene:368, lld:C0035435;
    a sio:SIO_001121 .
}

dgn-np:NP696108.RAX3gWURgWCspjYhLiHj22gxL45e5ITfPgAQUAjDLRsXw130_provenance {
  dgn-np:NP696108.RAX3gWURgWCspjYhLiHj22gxL45e5ITfPgAQUAjDLRsXw130_assertion dcterms:description
      "[951 RA cases in the UK satisfying American Rheumatism Association (ARA) criteria and 448 population controls were genotyped for 11 SNPs across the PTPN22 gene region using the Sequenom MassArray MassEXTEND technology.]. 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:17170052;
    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:NP696108.RAX3gWURgWCspjYhLiHj22gxL45e5ITfPgAQUAjDLRsXw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:03+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" .
}