@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP332980.RACbl__ebxnUh_StwWEpVLoT7MJSfx3CK9MBknxi1khdE> .
@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:NP332980.RACbl__ebxnUh_StwWEpVLoT7MJSfx3CK9MBknxi1khdE130_head {
  this: np:hasAssertion dgn-np:NP332980.RACbl__ebxnUh_StwWEpVLoT7MJSfx3CK9MBknxi1khdE130_assertion;
    np:hasProvenance dgn-np:NP332980.RACbl__ebxnUh_StwWEpVLoT7MJSfx3CK9MBknxi1khdE130_provenance;
    np:hasPublicationInfo dgn-np:NP332980.RACbl__ebxnUh_StwWEpVLoT7MJSfx3CK9MBknxi1khdE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP332980.RACbl__ebxnUh_StwWEpVLoT7MJSfx3CK9MBknxi1khdE130_assertion a np:Assertion .
  
  dgn-np:NP332980.RACbl__ebxnUh_StwWEpVLoT7MJSfx3CK9MBknxi1khdE130_provenance a np:Provenance .
  
  dgn-np:NP332980.RACbl__ebxnUh_StwWEpVLoT7MJSfx3CK9MBknxi1khdE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP332980.RACbl__ebxnUh_StwWEpVLoT7MJSfx3CK9MBknxi1khdE130_assertion {
  miriam-gene:4763 a ncit:C16612 .
  
  lld:C0017075 a ncit:C7057 .
  
  dgn-gda:DGN5e1bb54e05d35c0f0eaa08921c4d8136 sio:SIO_000628 miriam-gene:4763, lld:C0017075;
    a sio:SIO_001121 .
}

dgn-np:NP332980.RACbl__ebxnUh_StwWEpVLoT7MJSfx3CK9MBknxi1khdE130_provenance {
  dgn-np:NP332980.RACbl__ebxnUh_StwWEpVLoT7MJSfx3CK9MBknxi1khdE130_assertion dcterms:description
      "[In addition to associations with neuroblastoma and tumours related to MEN2B, HSCR may also be associated with tumours of neural origin such as ganglioneuroma, ganglioneuroblastoma, retinoblastoma and tumours associated with neurofibromatosis and other autonomic nervous system disturbances.]. 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:16518596;
    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:NP332980.RACbl__ebxnUh_StwWEpVLoT7MJSfx3CK9MBknxi1khdE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:16+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" .
}