@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP900699.RA9AGml2X0NgJT1emCgF2y9_ytalIFarvuxxnakiWVrE8> .
@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:NP900699.RA9AGml2X0NgJT1emCgF2y9_ytalIFarvuxxnakiWVrE8130_head {
  this: np:hasAssertion dgn-np:NP900699.RA9AGml2X0NgJT1emCgF2y9_ytalIFarvuxxnakiWVrE8130_assertion;
    np:hasProvenance dgn-np:NP900699.RA9AGml2X0NgJT1emCgF2y9_ytalIFarvuxxnakiWVrE8130_provenance;
    np:hasPublicationInfo dgn-np:NP900699.RA9AGml2X0NgJT1emCgF2y9_ytalIFarvuxxnakiWVrE8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP900699.RA9AGml2X0NgJT1emCgF2y9_ytalIFarvuxxnakiWVrE8130_assertion a np:Assertion .
  
  dgn-np:NP900699.RA9AGml2X0NgJT1emCgF2y9_ytalIFarvuxxnakiWVrE8130_provenance a np:Provenance .
  
  dgn-np:NP900699.RA9AGml2X0NgJT1emCgF2y9_ytalIFarvuxxnakiWVrE8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP900699.RA9AGml2X0NgJT1emCgF2y9_ytalIFarvuxxnakiWVrE8130_assertion {
  miriam-gene:8996 a ncit:C16612 .
  
  lld:C0027651 a ncit:C7057 .
  
  dgn-gda:DGNa7451fb81f0848b825364a968ed103fa sio:SIO_000628 miriam-gene:8996, lld:C0027651;
    a sio:SIO_001121 .
}

dgn-np:NP900699.RA9AGml2X0NgJT1emCgF2y9_ytalIFarvuxxnakiWVrE8130_provenance {
  dgn-np:NP900699.RA9AGml2X0NgJT1emCgF2y9_ytalIFarvuxxnakiWVrE8130_assertion dcterms:description
      "[While our results suggest that interactive IA is potentially a more sensitive method than FCM for detecting aneuploidy in cutaneous pigmented lesions, it remains to be shown whether this will translate into better prognostic assessment of the biologic behavior of melanocytic neoplasms than provided by flow cytometric ploidy analysis.]. 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:1558616;
    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:NP900699.RA9AGml2X0NgJT1emCgF2y9_ytalIFarvuxxnakiWVrE8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:13+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" .
}