@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP769715.RAVIb8Mg6d29qrMLEX1qz2ecdS26H36WqbvVZAU7TuQrI> .
@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:NP769715.RAVIb8Mg6d29qrMLEX1qz2ecdS26H36WqbvVZAU7TuQrI130_head {
  this: np:hasAssertion dgn-np:NP769715.RAVIb8Mg6d29qrMLEX1qz2ecdS26H36WqbvVZAU7TuQrI130_assertion;
    np:hasProvenance dgn-np:NP769715.RAVIb8Mg6d29qrMLEX1qz2ecdS26H36WqbvVZAU7TuQrI130_provenance;
    np:hasPublicationInfo dgn-np:NP769715.RAVIb8Mg6d29qrMLEX1qz2ecdS26H36WqbvVZAU7TuQrI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP769715.RAVIb8Mg6d29qrMLEX1qz2ecdS26H36WqbvVZAU7TuQrI130_assertion a np:Assertion .
  
  dgn-np:NP769715.RAVIb8Mg6d29qrMLEX1qz2ecdS26H36WqbvVZAU7TuQrI130_provenance a np:Provenance .
  
  dgn-np:NP769715.RAVIb8Mg6d29qrMLEX1qz2ecdS26H36WqbvVZAU7TuQrI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP769715.RAVIb8Mg6d29qrMLEX1qz2ecdS26H36WqbvVZAU7TuQrI130_assertion {
  miriam-gene:5300 a ncit:C16612 .
  
  lld:C1168401 a ncit:C7057 .
  
  dgn-gda:DGNc869d2b83ba690a530d32b72c18ffc9f sio:SIO_000628 miriam-gene:5300, lld:C1168401;
    a sio:SIO_001121 .
}

dgn-np:NP769715.RAVIb8Mg6d29qrMLEX1qz2ecdS26H36WqbvVZAU7TuQrI130_provenance {
  dgn-np:NP769715.RAVIb8Mg6d29qrMLEX1qz2ecdS26H36WqbvVZAU7TuQrI130_assertion dcterms:description
      "[In this study, we tested the hypothesis that common polymorphisms in the coding and promoter regions of PIN1 are associated with risk of squamous cell carcinoma of the head and neck (SCCHN).]. 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:19625347;
    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:NP769715.RAVIb8Mg6d29qrMLEX1qz2ecdS26H36WqbvVZAU7TuQrI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:45+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" .
}