@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP50547.RAGII16_jEtwuFd90z9wTu7qbhQ53OnVsPr1jKW0PLjSc> .
@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:NP50547.RAGII16_jEtwuFd90z9wTu7qbhQ53OnVsPr1jKW0PLjSc130_head {
  this: np:hasAssertion dgn-np:NP50547.RAGII16_jEtwuFd90z9wTu7qbhQ53OnVsPr1jKW0PLjSc130_assertion;
    np:hasProvenance dgn-np:NP50547.RAGII16_jEtwuFd90z9wTu7qbhQ53OnVsPr1jKW0PLjSc130_provenance;
    np:hasPublicationInfo dgn-np:NP50547.RAGII16_jEtwuFd90z9wTu7qbhQ53OnVsPr1jKW0PLjSc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP50547.RAGII16_jEtwuFd90z9wTu7qbhQ53OnVsPr1jKW0PLjSc130_assertion a np:Assertion .
  
  dgn-np:NP50547.RAGII16_jEtwuFd90z9wTu7qbhQ53OnVsPr1jKW0PLjSc130_provenance a np:Provenance .
  
  dgn-np:NP50547.RAGII16_jEtwuFd90z9wTu7qbhQ53OnVsPr1jKW0PLjSc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP50547.RAGII16_jEtwuFd90z9wTu7qbhQ53OnVsPr1jKW0PLjSc130_assertion {
  miriam-gene:7048 a ncit:C16612 .
  
  lld:C0024623 a ncit:C7057 .
  
  dgn-gda:DGNb01b2c056d0dd786347b3a53aafe32ce sio:SIO_000628 miriam-gene:7048, lld:C0024623;
    a sio:SIO_001122 .
}

dgn-np:NP50547.RAGII16_jEtwuFd90z9wTu7qbhQ53OnVsPr1jKW0PLjSc130_provenance {
  dgn-np:NP50547.RAGII16_jEtwuFd90z9wTu7qbhQ53OnVsPr1jKW0PLjSc130_assertion dcterms:description
      "[ These results indicate that the acquisition of the RER phenotype equally influences the gastric carcinogenesis of both sporadic and familial cases, and that the majority of FGC is pathogenetically distinct from HNPCC.]. 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:9498272;
    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:NP50547.RAGII16_jEtwuFd90z9wTu7qbhQ53OnVsPr1jKW0PLjSc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:23+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" .
}