@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP689339.RAGBcP732Hah6oTdRfOIKO2xQi-crfc6cUuwIi5hiIVM0> .
@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:NP689339.RAGBcP732Hah6oTdRfOIKO2xQi-crfc6cUuwIi5hiIVM0130_head {
  this: np:hasAssertion dgn-np:NP689339.RAGBcP732Hah6oTdRfOIKO2xQi-crfc6cUuwIi5hiIVM0130_assertion;
    np:hasProvenance dgn-np:NP689339.RAGBcP732Hah6oTdRfOIKO2xQi-crfc6cUuwIi5hiIVM0130_provenance;
    np:hasPublicationInfo dgn-np:NP689339.RAGBcP732Hah6oTdRfOIKO2xQi-crfc6cUuwIi5hiIVM0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP689339.RAGBcP732Hah6oTdRfOIKO2xQi-crfc6cUuwIi5hiIVM0130_assertion a np:Assertion .
  
  dgn-np:NP689339.RAGBcP732Hah6oTdRfOIKO2xQi-crfc6cUuwIi5hiIVM0130_provenance a np:Provenance .
  
  dgn-np:NP689339.RAGBcP732Hah6oTdRfOIKO2xQi-crfc6cUuwIi5hiIVM0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP689339.RAGBcP732Hah6oTdRfOIKO2xQi-crfc6cUuwIi5hiIVM0130_assertion {
  miriam-gene:8581 a ncit:C16612 .
  
  lld:C0268074 a ncit:C7057 .
  
  dgn-gda:DGN4c8c2aa752b84163bde1c874e22994d3 sio:SIO_000628 miriam-gene:8581, lld:C0268074;
    a sio:SIO_001121 .
}

dgn-np:NP689339.RAGBcP732Hah6oTdRfOIKO2xQi-crfc6cUuwIi5hiIVM0130_provenance {
  dgn-np:NP689339.RAGBcP732Hah6oTdRfOIKO2xQi-crfc6cUuwIi5hiIVM0130_assertion dcterms:description
      "[The concordance between the molecular and ICC tests applied to preoperative samples, measured by Cohen's kappa, was not uniformly good, which likely reflected sampling errors, heterogeneity of E48 antigen expression, or stochastic effects.]. 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:14614011;
    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:NP689339.RAGBcP732Hah6oTdRfOIKO2xQi-crfc6cUuwIi5hiIVM0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:59+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" .
}