@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP509746.RAPwfgDAsOHMW4G2ZX7WpYXzzo2i9rvKX9leTU88ifrUY> .
@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:NP509746.RAPwfgDAsOHMW4G2ZX7WpYXzzo2i9rvKX9leTU88ifrUY130_head {
  this: np:hasAssertion dgn-np:NP509746.RAPwfgDAsOHMW4G2ZX7WpYXzzo2i9rvKX9leTU88ifrUY130_assertion ;
    np:hasProvenance dgn-np:NP509746.RAPwfgDAsOHMW4G2ZX7WpYXzzo2i9rvKX9leTU88ifrUY130_provenance ;
    np:hasPublicationInfo dgn-np:NP509746.RAPwfgDAsOHMW4G2ZX7WpYXzzo2i9rvKX9leTU88ifrUY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP509746.RAPwfgDAsOHMW4G2ZX7WpYXzzo2i9rvKX9leTU88ifrUY130_assertion a np:Assertion .
  dgn-np:NP509746.RAPwfgDAsOHMW4G2ZX7WpYXzzo2i9rvKX9leTU88ifrUY130_provenance a np:Provenance .
  dgn-np:NP509746.RAPwfgDAsOHMW4G2ZX7WpYXzzo2i9rvKX9leTU88ifrUY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP509746.RAPwfgDAsOHMW4G2ZX7WpYXzzo2i9rvKX9leTU88ifrUY130_assertion {
  miriam-gene:1956 a ncit:C16612 .
  lld:C0008626 a ncit:C7057 .
  dgn-gda:DGN9c095a28b4cb6826268add19fcfa7ec1 sio:SIO_000628 miriam-gene:1956 , lld:C0008626 ;
    a sio:SIO_001121 .
}
dgn-np:NP509746.RAPwfgDAsOHMW4G2ZX7WpYXzzo2i9rvKX9leTU88ifrUY130_provenance {
  dgn-np:NP509746.RAPwfgDAsOHMW4G2ZX7WpYXzzo2i9rvKX9leTU88ifrUY130_assertion dcterms:description "[The global analysis of amplification afforded by aCGH analysis has improved our ability to define numerical chromosome abnormalities in cancer cells and has raised the possibility that genes other than EGFR may be important.]. 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:16110500 ;
    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:NP509746.RAPwfgDAsOHMW4G2ZX7WpYXzzo2i9rvKX9leTU88ifrUY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:36+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" .
}