@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP674680.RAsK1lpZdkg2ptyH931IcwbVeb64XNOnBb3t3_B5B0aJU> .
@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:NP674680.RAsK1lpZdkg2ptyH931IcwbVeb64XNOnBb3t3_B5B0aJU130_head {
  this: np:hasAssertion dgn-np:NP674680.RAsK1lpZdkg2ptyH931IcwbVeb64XNOnBb3t3_B5B0aJU130_assertion;
    np:hasProvenance dgn-np:NP674680.RAsK1lpZdkg2ptyH931IcwbVeb64XNOnBb3t3_B5B0aJU130_provenance;
    np:hasPublicationInfo dgn-np:NP674680.RAsK1lpZdkg2ptyH931IcwbVeb64XNOnBb3t3_B5B0aJU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP674680.RAsK1lpZdkg2ptyH931IcwbVeb64XNOnBb3t3_B5B0aJU130_assertion a np:Assertion .
  
  dgn-np:NP674680.RAsK1lpZdkg2ptyH931IcwbVeb64XNOnBb3t3_B5B0aJU130_provenance a np:Provenance .
  
  dgn-np:NP674680.RAsK1lpZdkg2ptyH931IcwbVeb64XNOnBb3t3_B5B0aJU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP674680.RAsK1lpZdkg2ptyH931IcwbVeb64XNOnBb3t3_B5B0aJU130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  
  lld:C0333875 a ncit:C7057 .
  
  dgn-gda:DGNdddaa15df1ba51782805b11cdc182843 sio:SIO_000628 miriam-gene:1029, lld:C0333875;
    a sio:SIO_001121 .
}

dgn-np:NP674680.RAsK1lpZdkg2ptyH931IcwbVeb64XNOnBb3t3_B5B0aJU130_provenance {
  dgn-np:NP674680.RAsK1lpZdkg2ptyH931IcwbVeb64XNOnBb3t3_B5B0aJU130_assertion dcterms:description
      "[The use of p16 immunostain in cytologic specimens applying the Wentzensen criteria helps to focus the attention in positive cells evaluating the cell changes, helps to detect some cells suspicious or diagnostic of HSIL, and could help to reclassify the ASCUS cases.]. 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:21254457;
    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:NP674680.RAsK1lpZdkg2ptyH931IcwbVeb64XNOnBb3t3_B5B0aJU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:47+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" .
}