@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP172803.RAhI7emZr_6meLTni_V8eRgDF3fB1pbXg4XrY6Un9yGkk> .
@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:NP172803.RAhI7emZr_6meLTni_V8eRgDF3fB1pbXg4XrY6Un9yGkk130_head {
  this: np:hasAssertion dgn-np:NP172803.RAhI7emZr_6meLTni_V8eRgDF3fB1pbXg4XrY6Un9yGkk130_assertion;
    np:hasProvenance dgn-np:NP172803.RAhI7emZr_6meLTni_V8eRgDF3fB1pbXg4XrY6Un9yGkk130_provenance;
    np:hasPublicationInfo dgn-np:NP172803.RAhI7emZr_6meLTni_V8eRgDF3fB1pbXg4XrY6Un9yGkk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP172803.RAhI7emZr_6meLTni_V8eRgDF3fB1pbXg4XrY6Un9yGkk130_assertion a np:Assertion .
  
  dgn-np:NP172803.RAhI7emZr_6meLTni_V8eRgDF3fB1pbXg4XrY6Un9yGkk130_provenance a np:Provenance .
  
  dgn-np:NP172803.RAhI7emZr_6meLTni_V8eRgDF3fB1pbXg4XrY6Un9yGkk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP172803.RAhI7emZr_6meLTni_V8eRgDF3fB1pbXg4XrY6Un9yGkk130_assertion {
  miriam-gene:4193 a ncit:C16612 .
  
  lld:C0029463 a ncit:C7057 .
  
  dgn-gda:DGN60c76b6af1583c113ced65a85fbaf625 sio:SIO_000628 miriam-gene:4193, lld:C0029463;
    a sio:SIO_001121 .
}

dgn-np:NP172803.RAhI7emZr_6meLTni_V8eRgDF3fB1pbXg4XrY6Un9yGkk130_provenance {
  dgn-np:NP172803.RAhI7emZr_6meLTni_V8eRgDF3fB1pbXg4XrY6Un9yGkk130_assertion dcterms:description
      "[In this study, 23 cases of OS (15 osteoblastic and 8 MFH-like types) and 18 cases of MFH of bone in patients 40 years of age or older were analyzed for mutation of the p53 gene, amplification of the MDM2 gene, and mutation of the H-ras gene, using formalin-fixed paraffin-embedded materials.]. 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:12181274;
    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:NP172803.RAhI7emZr_6meLTni_V8eRgDF3fB1pbXg4XrY6Un9yGkk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:33+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" .
}