@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP936433.RAjeS8fT9uU9KYPfY3zguB9he8KwibaZb4SAYIGFrRWEI> .
@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:NP936433.RAjeS8fT9uU9KYPfY3zguB9he8KwibaZb4SAYIGFrRWEI130_head {
  this: np:hasAssertion dgn-np:NP936433.RAjeS8fT9uU9KYPfY3zguB9he8KwibaZb4SAYIGFrRWEI130_assertion;
    np:hasProvenance dgn-np:NP936433.RAjeS8fT9uU9KYPfY3zguB9he8KwibaZb4SAYIGFrRWEI130_provenance;
    np:hasPublicationInfo dgn-np:NP936433.RAjeS8fT9uU9KYPfY3zguB9he8KwibaZb4SAYIGFrRWEI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP936433.RAjeS8fT9uU9KYPfY3zguB9he8KwibaZb4SAYIGFrRWEI130_assertion a np:Assertion .
  
  dgn-np:NP936433.RAjeS8fT9uU9KYPfY3zguB9he8KwibaZb4SAYIGFrRWEI130_provenance a np:Provenance .
  
  dgn-np:NP936433.RAjeS8fT9uU9KYPfY3zguB9he8KwibaZb4SAYIGFrRWEI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP936433.RAjeS8fT9uU9KYPfY3zguB9he8KwibaZb4SAYIGFrRWEI130_assertion {
  miriam-gene:4771 a ncit:C16612 .
  
  lld:C0596263 a ncit:C7057 .
  
  dgn-gda:DGNaf47a786ad97c6b60483a12a2d986449 sio:SIO_000628 miriam-gene:4771, lld:C0596263;
    a sio:SIO_001121 .
}

dgn-np:NP936433.RAjeS8fT9uU9KYPfY3zguB9he8KwibaZb4SAYIGFrRWEI130_provenance {
  dgn-np:NP936433.RAjeS8fT9uU9KYPfY3zguB9he8KwibaZb4SAYIGFrRWEI130_assertion dcterms:description
      "[In order to examine the significance of NF2 in general carcinogenesis, comprehensive analyses of 68 cases of breast carcinoma, which shows frequent loss of heterozygosity at chromosome 22, and 48 hepatocellular carcinomas of different histological grade were performed.]. 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:7877257;
    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:NP936433.RAjeS8fT9uU9KYPfY3zguB9he8KwibaZb4SAYIGFrRWEI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:34+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" .
}