@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1354031.RAOgXmqhwzLnvTRS8pj_R6hiDQvzDjORwTnf_0pnWy_hY> .
@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:NP1354031.RAOgXmqhwzLnvTRS8pj_R6hiDQvzDjORwTnf_0pnWy_hY130_head {
  this: np:hasAssertion dgn-np:NP1354031.RAOgXmqhwzLnvTRS8pj_R6hiDQvzDjORwTnf_0pnWy_hY130_assertion;
    np:hasProvenance dgn-np:NP1354031.RAOgXmqhwzLnvTRS8pj_R6hiDQvzDjORwTnf_0pnWy_hY130_provenance;
    np:hasPublicationInfo dgn-np:NP1354031.RAOgXmqhwzLnvTRS8pj_R6hiDQvzDjORwTnf_0pnWy_hY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1354031.RAOgXmqhwzLnvTRS8pj_R6hiDQvzDjORwTnf_0pnWy_hY130_assertion a np:Assertion .
  
  dgn-np:NP1354031.RAOgXmqhwzLnvTRS8pj_R6hiDQvzDjORwTnf_0pnWy_hY130_provenance a np:Provenance .
  
  dgn-np:NP1354031.RAOgXmqhwzLnvTRS8pj_R6hiDQvzDjORwTnf_0pnWy_hY130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1354031.RAOgXmqhwzLnvTRS8pj_R6hiDQvzDjORwTnf_0pnWy_hY130_assertion {
  miriam-gene:4771 a ncit:C16612 .
  
  lld:C0027832 a ncit:C7057 .
  
  dgn-gda:DGN0932b318f3c0aa1e9d07ac4cab8fc8b3 sio:SIO_000628 miriam-gene:4771, lld:C0027832;
    a sio:SIO_001121 .
}

dgn-np:NP1354031.RAOgXmqhwzLnvTRS8pj_R6hiDQvzDjORwTnf_0pnWy_hY130_provenance {
  dgn-np:NP1354031.RAOgXmqhwzLnvTRS8pj_R6hiDQvzDjORwTnf_0pnWy_hY130_assertion dcterms:description
      "[Furthermore, malignant human tumours seemingly unrelated to the NF2 syndrome, such as malignant melanomas (derived from the neural crest) and malignant mesotheliomas (derived from pleural mesoderm), also frequently have mutations or deletions at the NF2 locus, suggesting a broader role of the NF2 gene in the initiation and progression of human neoplasms.]. 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:8718520;
    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:NP1354031.RAOgXmqhwzLnvTRS8pj_R6hiDQvzDjORwTnf_0pnWy_hY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:00+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" .
}