@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP751677.RAp2n0b-WgaPDBp8H_EtPUZvrx3qJcj1JYOiLHdAcOBoM> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP751677.RAp2n0b-WgaPDBp8H_EtPUZvrx3qJcj1JYOiLHdAcOBoM130_head {
  this: np:hasAssertion dgn-np:NP751677.RAp2n0b-WgaPDBp8H_EtPUZvrx3qJcj1JYOiLHdAcOBoM130_assertion;
    np:hasProvenance dgn-np:NP751677.RAp2n0b-WgaPDBp8H_EtPUZvrx3qJcj1JYOiLHdAcOBoM130_provenance;
    np:hasPublicationInfo dgn-np:NP751677.RAp2n0b-WgaPDBp8H_EtPUZvrx3qJcj1JYOiLHdAcOBoM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP751677.RAp2n0b-WgaPDBp8H_EtPUZvrx3qJcj1JYOiLHdAcOBoM130_assertion a np:Assertion .
  
  dgn-np:NP751677.RAp2n0b-WgaPDBp8H_EtPUZvrx3qJcj1JYOiLHdAcOBoM130_provenance a np:Provenance .
  
  dgn-np:NP751677.RAp2n0b-WgaPDBp8H_EtPUZvrx3qJcj1JYOiLHdAcOBoM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP751677.RAp2n0b-WgaPDBp8H_EtPUZvrx3qJcj1JYOiLHdAcOBoM130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0153381 a ncit:C7057 .
  
  dgn-gda:DGNf428d98b911203d28b9cd896cf976077 sio:SIO_000628 miriam-gene:7157, lld:C0153381;
    a sio:SIO_001121 .
}

dgn-np:NP751677.RAp2n0b-WgaPDBp8H_EtPUZvrx3qJcj1JYOiLHdAcOBoM130_provenance {
  dgn-np:NP751677.RAp2n0b-WgaPDBp8H_EtPUZvrx3qJcj1JYOiLHdAcOBoM130_assertion dcterms:description
      "[Out of the 349 genes, 34 (including several S100 gene family members) were found to be deleted and 30 (containing NOTCH4, TP53 and ERBB2) were found as amplified in OSF and OC cases.]. 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:24969693;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP751677.RAp2n0b-WgaPDBp8H_EtPUZvrx3qJcj1JYOiLHdAcOBoM130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:13+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}