@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP829367.RAKHJVSEOFCdlhv32R7Xt0FuutI-6EfVh4SSj9r6OBT84> .
@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:NP829367.RAKHJVSEOFCdlhv32R7Xt0FuutI-6EfVh4SSj9r6OBT84130_head {
  this: np:hasAssertion dgn-np:NP829367.RAKHJVSEOFCdlhv32R7Xt0FuutI-6EfVh4SSj9r6OBT84130_assertion;
    np:hasProvenance dgn-np:NP829367.RAKHJVSEOFCdlhv32R7Xt0FuutI-6EfVh4SSj9r6OBT84130_provenance;
    np:hasPublicationInfo dgn-np:NP829367.RAKHJVSEOFCdlhv32R7Xt0FuutI-6EfVh4SSj9r6OBT84130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP829367.RAKHJVSEOFCdlhv32R7Xt0FuutI-6EfVh4SSj9r6OBT84130_assertion a np:Assertion .
  
  dgn-np:NP829367.RAKHJVSEOFCdlhv32R7Xt0FuutI-6EfVh4SSj9r6OBT84130_provenance a np:Provenance .
  
  dgn-np:NP829367.RAKHJVSEOFCdlhv32R7Xt0FuutI-6EfVh4SSj9r6OBT84130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP829367.RAKHJVSEOFCdlhv32R7Xt0FuutI-6EfVh4SSj9r6OBT84130_assertion {
  miriam-gene:8718 a ncit:C16612 .
  
  lld:C0220633 a ncit:C7057 .
  
  dgn-gda:DGN41954e45aa7d53ba3e60c9e55cee0551 sio:SIO_000628 miriam-gene:8718, lld:C0220633;
    a sio:SIO_001121 .
}

dgn-np:NP829367.RAKHJVSEOFCdlhv32R7Xt0FuutI-6EfVh4SSj9r6OBT84130_provenance {
  dgn-np:NP829367.RAKHJVSEOFCdlhv32R7Xt0FuutI-6EfVh4SSj9r6OBT84130_assertion dcterms:description
      "[The deviated frequencies of class I HLA antigens (A32, B27) seem to be involved in the predisposition to spindle cell melanoma, while HLA class II (DR3, DR7) and class III (Bf F) strongly mark the worst form of UM.]. 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:3180122;
    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:NP829367.RAKHJVSEOFCdlhv32R7Xt0FuutI-6EfVh4SSj9r6OBT84130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:27+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" .
}