@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP634731.RAP96UecWEpXApEm6xVTaDkGcCszkdx-zQSPb2MFMUl6E> .
@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:NP634731.RAP96UecWEpXApEm6xVTaDkGcCszkdx-zQSPb2MFMUl6E130_head {
  this: np:hasAssertion dgn-np:NP634731.RAP96UecWEpXApEm6xVTaDkGcCszkdx-zQSPb2MFMUl6E130_assertion;
    np:hasProvenance dgn-np:NP634731.RAP96UecWEpXApEm6xVTaDkGcCszkdx-zQSPb2MFMUl6E130_provenance;
    np:hasPublicationInfo dgn-np:NP634731.RAP96UecWEpXApEm6xVTaDkGcCszkdx-zQSPb2MFMUl6E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP634731.RAP96UecWEpXApEm6xVTaDkGcCszkdx-zQSPb2MFMUl6E130_assertion a np:Assertion .
  
  dgn-np:NP634731.RAP96UecWEpXApEm6xVTaDkGcCszkdx-zQSPb2MFMUl6E130_provenance a np:Provenance .
  
  dgn-np:NP634731.RAP96UecWEpXApEm6xVTaDkGcCszkdx-zQSPb2MFMUl6E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP634731.RAP96UecWEpXApEm6xVTaDkGcCszkdx-zQSPb2MFMUl6E130_assertion {
  miriam-gene:1557 a ncit:C16612 .
  
  lld:C0017154 a ncit:C7057 .
  
  dgn-gda:DGN527dd277d83b01a1758f8c40c50cb470 sio:SIO_000628 miriam-gene:1557, lld:C0017154;
    a sio:SIO_001121 .
}

dgn-np:NP634731.RAP96UecWEpXApEm6xVTaDkGcCszkdx-zQSPb2MFMUl6E130_provenance {
  dgn-np:NP634731.RAP96UecWEpXApEm6xVTaDkGcCszkdx-zQSPb2MFMUl6E130_assertion dcterms:description
      "[SNPs rs9315542 (UFM1 gene), rs6878265 (THBS4 gene), rs1042194 (CYP2C19 gene) and rs10505799 (MGST1 gene) were significantly associated with atrophic gastritis, complete intestinal metaplasia, incomplete metaplasia with foci of dysplasia and dysplasia, respectively.]. 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:23801863;
    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:NP634731.RAP96UecWEpXApEm6xVTaDkGcCszkdx-zQSPb2MFMUl6E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:23+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" .
}