@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1309726.RACSxbkRstSq2bxCVfGPVN8cA5222A8wpam8fno96tw5o> .
@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/v4.0.0/void/> .
dgn-np:NP1309726.RACSxbkRstSq2bxCVfGPVN8cA5222A8wpam8fno96tw5o130_head {
   this: np:hasAssertion dgn-np:NP1309726.RACSxbkRstSq2bxCVfGPVN8cA5222A8wpam8fno96tw5o130_assertion ;
    np:hasProvenance dgn-np:NP1309726.RACSxbkRstSq2bxCVfGPVN8cA5222A8wpam8fno96tw5o130_provenance ;
    np:hasPublicationInfo dgn-np:NP1309726.RACSxbkRstSq2bxCVfGPVN8cA5222A8wpam8fno96tw5o130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1309726.RACSxbkRstSq2bxCVfGPVN8cA5222A8wpam8fno96tw5o130_assertion a np:Assertion .
  dgn-np:NP1309726.RACSxbkRstSq2bxCVfGPVN8cA5222A8wpam8fno96tw5o130_provenance a np:Provenance .
  dgn-np:NP1309726.RACSxbkRstSq2bxCVfGPVN8cA5222A8wpam8fno96tw5o130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1309726.RACSxbkRstSq2bxCVfGPVN8cA5222A8wpam8fno96tw5o130_assertion {
   miriam-gene:1956 a ncit:C16612 .
  lld:C0004114 a ncit:C7057 .
  dgn-gda:DGN02e12e71326fd347815ac95c069db9ad sio:SIO_000628 miriam-gene:1956 , lld:C0004114 ;
    a sio:SIO_001121 .
}
dgn-np:NP1309726.RACSxbkRstSq2bxCVfGPVN8cA5222A8wpam8fno96tw5o130_provenance {
   dgn-np:NP1309726.RACSxbkRstSq2bxCVfGPVN8cA5222A8wpam8fno96tw5o130_assertion dcterms:description "[Loss of heterozygosity (LOH) for chromosome arms 9p, 10p, 10q, and 17p and amplification of the epidermal growth factor receptor (EGFR) gene have been identified as frequent genetic changes in malignant astrocytomas.]. 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:7513547 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1309726.RACSxbkRstSq2bxCVfGPVN8cA5222A8wpam8fno96tw5o130_publicationInfo {
   this: dcterms:created "2016-05-13T12:51:39+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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}