@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1323093.RAhiCHUBA7reWLg6_cjfHKhbhjtlj7t6VpFOmI4NzkjUI> .
@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:NP1323093.RAhiCHUBA7reWLg6_cjfHKhbhjtlj7t6VpFOmI4NzkjUI130_head {
  this: np:hasAssertion dgn-np:NP1323093.RAhiCHUBA7reWLg6_cjfHKhbhjtlj7t6VpFOmI4NzkjUI130_assertion;
    np:hasProvenance dgn-np:NP1323093.RAhiCHUBA7reWLg6_cjfHKhbhjtlj7t6VpFOmI4NzkjUI130_provenance;
    np:hasPublicationInfo dgn-np:NP1323093.RAhiCHUBA7reWLg6_cjfHKhbhjtlj7t6VpFOmI4NzkjUI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1323093.RAhiCHUBA7reWLg6_cjfHKhbhjtlj7t6VpFOmI4NzkjUI130_assertion a np:Assertion .
  
  dgn-np:NP1323093.RAhiCHUBA7reWLg6_cjfHKhbhjtlj7t6VpFOmI4NzkjUI130_provenance a np:Provenance .
  
  dgn-np:NP1323093.RAhiCHUBA7reWLg6_cjfHKhbhjtlj7t6VpFOmI4NzkjUI130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1323093.RAhiCHUBA7reWLg6_cjfHKhbhjtlj7t6VpFOmI4NzkjUI130_assertion {
  miriam-gene:4763 a ncit:C16612 .
  
  lld:C0751690 a ncit:C7057 .
  
  dgn-gda:DGN2377426fedd4c74eea83d600d61285ae sio:SIO_000628 miriam-gene:4763, lld:C0751690;
    a sio:SIO_001121 .
}

dgn-np:NP1323093.RAhiCHUBA7reWLg6_cjfHKhbhjtlj7t6VpFOmI4NzkjUI130_provenance {
  dgn-np:NP1323093.RAhiCHUBA7reWLg6_cjfHKhbhjtlj7t6VpFOmI4NzkjUI130_assertion dcterms:description
      "[This study suggests that the germline mutation in one of the copies accompanied by loss or inactivation of the second copy of the NF1 gene and tumor suppressor gene(s) on 17p and 22q may be associated with the neoplastic transformation; abnormalities of other chromosomes may be related to progression of MPNST.]. 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:7828144;
    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:NP1323093.RAhiCHUBA7reWLg6_cjfHKhbhjtlj7t6VpFOmI4NzkjUI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:46+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}