@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP771876.RAqlKt0g7ikk-lFLF3vo-sP9JdMnIKQ0K-LXYA4W2vMBU> .
@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:NP771876.RAqlKt0g7ikk-lFLF3vo-sP9JdMnIKQ0K-LXYA4W2vMBU130_head {
  this: np:hasAssertion dgn-np:NP771876.RAqlKt0g7ikk-lFLF3vo-sP9JdMnIKQ0K-LXYA4W2vMBU130_assertion;
    np:hasProvenance dgn-np:NP771876.RAqlKt0g7ikk-lFLF3vo-sP9JdMnIKQ0K-LXYA4W2vMBU130_provenance;
    np:hasPublicationInfo dgn-np:NP771876.RAqlKt0g7ikk-lFLF3vo-sP9JdMnIKQ0K-LXYA4W2vMBU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP771876.RAqlKt0g7ikk-lFLF3vo-sP9JdMnIKQ0K-LXYA4W2vMBU130_assertion a np:Assertion .
  
  dgn-np:NP771876.RAqlKt0g7ikk-lFLF3vo-sP9JdMnIKQ0K-LXYA4W2vMBU130_provenance a np:Provenance .
  
  dgn-np:NP771876.RAqlKt0g7ikk-lFLF3vo-sP9JdMnIKQ0K-LXYA4W2vMBU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP771876.RAqlKt0g7ikk-lFLF3vo-sP9JdMnIKQ0K-LXYA4W2vMBU130_assertion {
  miriam-gene:7248 a ncit:C16612 .
  
  lld:C1168327 a ncit:C7057 .
  
  dgn-gda:DGNf6b594c273d118f5ddbd7c0b161b9c25 sio:SIO_000628 miriam-gene:7248, lld:C1168327;
    a sio:SIO_001121 .
}

dgn-np:NP771876.RAqlKt0g7ikk-lFLF3vo-sP9JdMnIKQ0K-LXYA4W2vMBU130_provenance {
  dgn-np:NP771876.RAqlKt0g7ikk-lFLF3vo-sP9JdMnIKQ0K-LXYA4W2vMBU130_assertion dcterms:description
      "[The combination of LCM, MDA and gaCGH is ideally suited for the identification of CNAs from small cell clusters and may assist in the discovery of potential genomic markers for early diagnosis, or identify the location of tumour suppressor genes (TSG) or oncogenes previously unreported in HPIN and CaP.]. 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:16573809;
    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:NP771876.RAqlKt0g7ikk-lFLF3vo-sP9JdMnIKQ0K-LXYA4W2vMBU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:47+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" .
}