@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP224989.RAS7zszcZHPEF_FibHBBNFWmVfqeRrGEXh-BSgpilHRQw> .
@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:NP224989.RAS7zszcZHPEF_FibHBBNFWmVfqeRrGEXh-BSgpilHRQw130_head {
  this: np:hasAssertion dgn-np:NP224989.RAS7zszcZHPEF_FibHBBNFWmVfqeRrGEXh-BSgpilHRQw130_assertion;
    np:hasProvenance dgn-np:NP224989.RAS7zszcZHPEF_FibHBBNFWmVfqeRrGEXh-BSgpilHRQw130_provenance;
    np:hasPublicationInfo dgn-np:NP224989.RAS7zszcZHPEF_FibHBBNFWmVfqeRrGEXh-BSgpilHRQw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP224989.RAS7zszcZHPEF_FibHBBNFWmVfqeRrGEXh-BSgpilHRQw130_assertion a np:Assertion .
  
  dgn-np:NP224989.RAS7zszcZHPEF_FibHBBNFWmVfqeRrGEXh-BSgpilHRQw130_provenance a np:Provenance .
  
  dgn-np:NP224989.RAS7zszcZHPEF_FibHBBNFWmVfqeRrGEXh-BSgpilHRQw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP224989.RAS7zszcZHPEF_FibHBBNFWmVfqeRrGEXh-BSgpilHRQw130_assertion {
  miriam-gene:2131 a ncit:C16612 .
  
  lld:C0206641 a ncit:C7057 .
  
  dgn-gda:DGN3a35b09a053cfe8f97d18af4677693aa sio:SIO_000628 miriam-gene:2131, lld:C0206641;
    a sio:SIO_001121 .
}

dgn-np:NP224989.RAS7zszcZHPEF_FibHBBNFWmVfqeRrGEXh-BSgpilHRQw130_provenance {
  dgn-np:NP224989.RAS7zszcZHPEF_FibHBBNFWmVfqeRrGEXh-BSgpilHRQw130_assertion dcterms:description
      "[The genetics of these tumors is intriguing ranging from single gene event (ie, EXT mutation in multiple osteochondromas) to heterogeneous rearrangements with no recurrent involved chromosomal regions such as in chondroblastoma.]. 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:19700940;
    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:NP224989.RAS7zszcZHPEF_FibHBBNFWmVfqeRrGEXh-BSgpilHRQw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:05+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" .
}