@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1245268.RAHMBjSEmrnsB4elWo8Vv5_T4ZbodiZ2PEhEgXSTTZD8k> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP1245268.RAHMBjSEmrnsB4elWo8Vv5_T4ZbodiZ2PEhEgXSTTZD8k130_head {
  this: np:hasAssertion dgn-np:NP1245268.RAHMBjSEmrnsB4elWo8Vv5_T4ZbodiZ2PEhEgXSTTZD8k130_assertion ;
    np:hasProvenance dgn-np:NP1245268.RAHMBjSEmrnsB4elWo8Vv5_T4ZbodiZ2PEhEgXSTTZD8k130_provenance ;
    np:hasPublicationInfo dgn-np:NP1245268.RAHMBjSEmrnsB4elWo8Vv5_T4ZbodiZ2PEhEgXSTTZD8k130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP1245268.RAHMBjSEmrnsB4elWo8Vv5_T4ZbodiZ2PEhEgXSTTZD8k130_provenance a np:Provenance .
  dgn-np:NP1245268.RAHMBjSEmrnsB4elWo8Vv5_T4ZbodiZ2PEhEgXSTTZD8k130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1245268.RAHMBjSEmrnsB4elWo8Vv5_T4ZbodiZ2PEhEgXSTTZD8k130_assertion {
  miriam-gene:8314 a ncit:C16612 .
  lld:C0220633 a ncit:C7057 .
  dgn-gda:DGNfa65e8401b61a5a6d0e9ada93e39ad04 sio:SIO_000628 miriam-gene:8314 , lld:C0220633 ;
    a sio:SIO_001121 .
}
dgn-np:NP1245268.RAHMBjSEmrnsB4elWo8Vv5_T4ZbodiZ2PEhEgXSTTZD8k130_provenance {
  dgn-np:NP1245268.RAHMBjSEmrnsB4elWo8Vv5_T4ZbodiZ2PEhEgXSTTZD8k130_assertion dcterms:description "[We investigated BAP1 and BRAFV600E expression in 193 sporadic melanocytic lesions (11 dermal nevi, 20 congenital nevi, 40 primary and nondesmoplastic melanomas, 40 desmoplastic melanomas, 23 metastatic melanomas, 17 Spitz nevi, 19 atypical Spitz nevi, 8 atypical Spitz tumors, 14 proliferative nodules arising in congenital nevi, 1 nevus during pregnancy) and 30 melanocytic lesions from 3 patients with family history of uveal melanoma and BAP1 germline mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1245268.RAHMBjSEmrnsB4elWo8Vv5_T4ZbodiZ2PEhEgXSTTZD8k130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:10+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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    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> ;
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}