@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP623960.RAGTz8Qewd4VaR9QB2CY7jDIod0kIB0qSEbww078gvmX8> .
@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:NP623960.RAGTz8Qewd4VaR9QB2CY7jDIod0kIB0qSEbww078gvmX8130_head {
  this: np:hasAssertion dgn-np:NP623960.RAGTz8Qewd4VaR9QB2CY7jDIod0kIB0qSEbww078gvmX8130_assertion ;
    np:hasProvenance dgn-np:NP623960.RAGTz8Qewd4VaR9QB2CY7jDIod0kIB0qSEbww078gvmX8130_provenance ;
    np:hasPublicationInfo dgn-np:NP623960.RAGTz8Qewd4VaR9QB2CY7jDIod0kIB0qSEbww078gvmX8130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP623960.RAGTz8Qewd4VaR9QB2CY7jDIod0kIB0qSEbww078gvmX8130_provenance a np:Provenance .
  dgn-np:NP623960.RAGTz8Qewd4VaR9QB2CY7jDIod0kIB0qSEbww078gvmX8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP623960.RAGTz8Qewd4VaR9QB2CY7jDIod0kIB0qSEbww078gvmX8130_assertion {
  miriam-gene:6045 a ncit:C16612 .
  lld:C0025500 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP623960.RAGTz8Qewd4VaR9QB2CY7jDIod0kIB0qSEbww078gvmX8130_provenance {
  dgn-np:NP623960.RAGTz8Qewd4VaR9QB2CY7jDIod0kIB0qSEbww078gvmX8130_assertion dcterms:description "[Recent findings indicate that germline BAP1 mutations cause a novel cancer syndrome that is characterized, at least in the affected families that have been studied so far, by the onset at an early age of benign melanocytic skin tumours with mutated BAP1, and later in life by a high incidence of mesothelioma, uveal melanoma, cutaneous melanoma and possibly additional cancers.]. 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:23550303 ;
    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 ;
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dgn-np:NP623960.RAGTz8Qewd4VaR9QB2CY7jDIod0kIB0qSEbww078gvmX8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:16+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 ;
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}