@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP499029.RAInV5r0fi0pc8yPtIDrCmkh2N14St5YH6sfcKw88em4g> .
@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:NP499029.RAInV5r0fi0pc8yPtIDrCmkh2N14St5YH6sfcKw88em4g130_head {
  this: np:hasAssertion dgn-np:NP499029.RAInV5r0fi0pc8yPtIDrCmkh2N14St5YH6sfcKw88em4g130_assertion ;
    np:hasProvenance dgn-np:NP499029.RAInV5r0fi0pc8yPtIDrCmkh2N14St5YH6sfcKw88em4g130_provenance ;
    np:hasPublicationInfo dgn-np:NP499029.RAInV5r0fi0pc8yPtIDrCmkh2N14St5YH6sfcKw88em4g130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP499029.RAInV5r0fi0pc8yPtIDrCmkh2N14St5YH6sfcKw88em4g130_assertion a np:Assertion .
  dgn-np:NP499029.RAInV5r0fi0pc8yPtIDrCmkh2N14St5YH6sfcKw88em4g130_provenance a np:Provenance .
  dgn-np:NP499029.RAInV5r0fi0pc8yPtIDrCmkh2N14St5YH6sfcKw88em4g130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP499029.RAInV5r0fi0pc8yPtIDrCmkh2N14St5YH6sfcKw88em4g130_assertion {
  miriam-gene:10142 a ncit:C16612 .
  lld:C0678222 a ncit:C7057 .
  dgn-gda:DGN3afe72d1023dc1127465b37ede51b60c sio:SIO_000628 miriam-gene:10142 , lld:C0678222 ;
    a sio:SIO_001121 .
}
dgn-np:NP499029.RAInV5r0fi0pc8yPtIDrCmkh2N14St5YH6sfcKw88em4g130_provenance {
  dgn-np:NP499029.RAInV5r0fi0pc8yPtIDrCmkh2N14St5YH6sfcKw88em4g130_assertion dcterms:description "[We extended the analysis of AKAP9 M463I, which is in strong linkage disequilibrium with AKAP9 N2792S, to 9523 breast cancer patients and 13770 healthy control subjects from seven independent European and Australian breast cancer studies.]. 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:18334708 ;
    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:NP499029.RAInV5r0fi0pc8yPtIDrCmkh2N14St5YH6sfcKw88em4g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:57+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" .
}