@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP62086.RAwyrUWvSlvpAyEzAIGKcjEmE7Eb_-qUpLWFW2MweOJIE> .
@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:NP62086.RAwyrUWvSlvpAyEzAIGKcjEmE7Eb_-qUpLWFW2MweOJIE130_head {
  this: np:hasAssertion dgn-np:NP62086.RAwyrUWvSlvpAyEzAIGKcjEmE7Eb_-qUpLWFW2MweOJIE130_assertion;
    np:hasProvenance dgn-np:NP62086.RAwyrUWvSlvpAyEzAIGKcjEmE7Eb_-qUpLWFW2MweOJIE130_provenance;
    np:hasPublicationInfo dgn-np:NP62086.RAwyrUWvSlvpAyEzAIGKcjEmE7Eb_-qUpLWFW2MweOJIE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP62086.RAwyrUWvSlvpAyEzAIGKcjEmE7Eb_-qUpLWFW2MweOJIE130_assertion a np:Assertion .
  
  dgn-np:NP62086.RAwyrUWvSlvpAyEzAIGKcjEmE7Eb_-qUpLWFW2MweOJIE130_provenance a np:Provenance .
  
  dgn-np:NP62086.RAwyrUWvSlvpAyEzAIGKcjEmE7Eb_-qUpLWFW2MweOJIE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP62086.RAwyrUWvSlvpAyEzAIGKcjEmE7Eb_-qUpLWFW2MweOJIE130_assertion {
  miriam-gene:7298 a ncit:C16612 .
  
  lld:C0024623 a ncit:C7057 .
  
  dgn-gda:DGN49f100886e096682675e8980a2208727 sio:SIO_000628 miriam-gene:7298, lld:C0024623;
    a sio:SIO_001122 .
}

dgn-np:NP62086.RAwyrUWvSlvpAyEzAIGKcjEmE7Eb_-qUpLWFW2MweOJIE130_provenance {
  dgn-np:NP62086.RAwyrUWvSlvpAyEzAIGKcjEmE7Eb_-qUpLWFW2MweOJIE130_assertion dcterms:description
      "[Polymorphisms in the TS gene may contribute to gastric cancer susceptibility and this finding deserve further investigation in the context of novel strategies for gastric cancer prevention. In vitro, 3G genotypes have been related to high TS mRNA expression, which may underlie one of the possible etiologic mechanisms.]. 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:15386366;
    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:NP62086.RAwyrUWvSlvpAyEzAIGKcjEmE7Eb_-qUpLWFW2MweOJIE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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" .
}