@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP787527.RAXNOnPGWpfB_BC7sAm9Xbi7FOeA2k6qTEcFzS4Nd6xPE> .
@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:NP787527.RAXNOnPGWpfB_BC7sAm9Xbi7FOeA2k6qTEcFzS4Nd6xPE130_head {
  this: np:hasAssertion dgn-np:NP787527.RAXNOnPGWpfB_BC7sAm9Xbi7FOeA2k6qTEcFzS4Nd6xPE130_assertion;
    np:hasProvenance dgn-np:NP787527.RAXNOnPGWpfB_BC7sAm9Xbi7FOeA2k6qTEcFzS4Nd6xPE130_provenance;
    np:hasPublicationInfo dgn-np:NP787527.RAXNOnPGWpfB_BC7sAm9Xbi7FOeA2k6qTEcFzS4Nd6xPE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP787527.RAXNOnPGWpfB_BC7sAm9Xbi7FOeA2k6qTEcFzS4Nd6xPE130_assertion a np:Assertion .
  
  dgn-np:NP787527.RAXNOnPGWpfB_BC7sAm9Xbi7FOeA2k6qTEcFzS4Nd6xPE130_provenance a np:Provenance .
  
  dgn-np:NP787527.RAXNOnPGWpfB_BC7sAm9Xbi7FOeA2k6qTEcFzS4Nd6xPE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP787527.RAXNOnPGWpfB_BC7sAm9Xbi7FOeA2k6qTEcFzS4Nd6xPE130_assertion {
  miriam-gene:3728 a ncit:C16612 .
  
  lld:C0677055 a ncit:C7057 .
  
  dgn-gda:DGN26b0249ad6b5295aea10f42c2f33d7b6 sio:SIO_000628 miriam-gene:3728, lld:C0677055;
    a sio:SIO_001121 .
}

dgn-np:NP787527.RAXNOnPGWpfB_BC7sAm9Xbi7FOeA2k6qTEcFzS4Nd6xPE130_provenance {
  dgn-np:NP787527.RAXNOnPGWpfB_BC7sAm9Xbi7FOeA2k6qTEcFzS4Nd6xPE130_assertion dcterms:description
      "[In the initial validation of the seven putative markers of metastatic LN, the Cox proportional hazard model pointed to SFN, CA12 and JUP expression to significantly relate to the time to groin recurrence in VC patients.]. 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:22673103;
    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:NP787527.RAXNOnPGWpfB_BC7sAm9Xbi7FOeA2k6qTEcFzS4Nd6xPE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:00+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" .
}