@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP549166.RAerJ1aou_VfoJcoygokBV7RYLwqv-w1bnmM5Snw0T32I> .
@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:NP549166.RAerJ1aou_VfoJcoygokBV7RYLwqv-w1bnmM5Snw0T32I130_head {
  this: np:hasAssertion dgn-np:NP549166.RAerJ1aou_VfoJcoygokBV7RYLwqv-w1bnmM5Snw0T32I130_assertion;
    np:hasProvenance dgn-np:NP549166.RAerJ1aou_VfoJcoygokBV7RYLwqv-w1bnmM5Snw0T32I130_provenance;
    np:hasPublicationInfo dgn-np:NP549166.RAerJ1aou_VfoJcoygokBV7RYLwqv-w1bnmM5Snw0T32I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP549166.RAerJ1aou_VfoJcoygokBV7RYLwqv-w1bnmM5Snw0T32I130_assertion a np:Assertion .
  
  dgn-np:NP549166.RAerJ1aou_VfoJcoygokBV7RYLwqv-w1bnmM5Snw0T32I130_provenance a np:Provenance .
  
  dgn-np:NP549166.RAerJ1aou_VfoJcoygokBV7RYLwqv-w1bnmM5Snw0T32I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP549166.RAerJ1aou_VfoJcoygokBV7RYLwqv-w1bnmM5Snw0T32I130_assertion {
  miriam-gene:613 a ncit:C16612 .
  
  lld:C0027832 a ncit:C7057 .
  
  dgn-gda:DGN293d34e057d03c934f31a6ef4c058ade sio:SIO_000628 miriam-gene:613, lld:C0027832;
    a sio:SIO_001121 .
}

dgn-np:NP549166.RAerJ1aou_VfoJcoygokBV7RYLwqv-w1bnmM5Snw0T32I130_provenance {
  dgn-np:NP549166.RAerJ1aou_VfoJcoygokBV7RYLwqv-w1bnmM5Snw0T32I130_assertion dcterms:description
      "[Archived and prospectively acquired tumor specimens were studied by mutational analysis at the NF2 locus, loss of heterozygosity analysis along chromosome 22, and fluorescent in situ hybridization analysis of NF2 and the more centromeric probe BCR.]. 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:12821741;
    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;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP549166.RAerJ1aou_VfoJcoygokBV7RYLwqv-w1bnmM5Snw0T32I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:31+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}