@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP588173.RApwrJKMmSSnqGebWtdEk7q9xOjS7hRbtBEtQP2nGU6yc> .
@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/v3.0.0/void/> .
dgn-np:NP588173.RApwrJKMmSSnqGebWtdEk7q9xOjS7hRbtBEtQP2nGU6yc130_head {
   this: np:hasAssertion dgn-np:NP588173.RApwrJKMmSSnqGebWtdEk7q9xOjS7hRbtBEtQP2nGU6yc130_assertion ;
    np:hasProvenance dgn-np:NP588173.RApwrJKMmSSnqGebWtdEk7q9xOjS7hRbtBEtQP2nGU6yc130_provenance ;
    np:hasPublicationInfo dgn-np:NP588173.RApwrJKMmSSnqGebWtdEk7q9xOjS7hRbtBEtQP2nGU6yc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP588173.RApwrJKMmSSnqGebWtdEk7q9xOjS7hRbtBEtQP2nGU6yc130_assertion a np:Assertion .
  dgn-np:NP588173.RApwrJKMmSSnqGebWtdEk7q9xOjS7hRbtBEtQP2nGU6yc130_provenance a np:Provenance .
  dgn-np:NP588173.RApwrJKMmSSnqGebWtdEk7q9xOjS7hRbtBEtQP2nGU6yc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP588173.RApwrJKMmSSnqGebWtdEk7q9xOjS7hRbtBEtQP2nGU6yc130_assertion {
   miriam-gene:4763 a ncit:C16612 .
  lld:C0027766 a ncit:C7057 .
  dgn-gda:DGN3ee8d80c469d5e672b9ff7b6a98ec69e sio:SIO_000628 miriam-gene:4763 , lld:C0027766 ;
    a sio:SIO_001121 .
}
dgn-np:NP588173.RApwrJKMmSSnqGebWtdEk7q9xOjS7hRbtBEtQP2nGU6yc130_provenance {
   dgn-np:NP588173.RApwrJKMmSSnqGebWtdEk7q9xOjS7hRbtBEtQP2nGU6yc130_assertion dcterms:description "[Loss of its protein, neurofibromin, in the autosomal dominant disorder NF1 is associated with peripheral nervous system tumors, particularly neurofibromas, benign lesions in which the major cell type is the Schwann Cell (SC).]. 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:18481270 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP588173.RApwrJKMmSSnqGebWtdEk7q9xOjS7hRbtBEtQP2nGU6yc130_publicationInfo {
   this: dcterms:created "2015-08-25T14:43:31+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}