@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP267474.RA7sChAUkLvk3P2E3cYCwFWN3F19Gp3QlnuE4cpyMPoeI> .
@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:NP267474.RA7sChAUkLvk3P2E3cYCwFWN3F19Gp3QlnuE4cpyMPoeI130_head {
  this: np:hasAssertion dgn-np:NP267474.RA7sChAUkLvk3P2E3cYCwFWN3F19Gp3QlnuE4cpyMPoeI130_assertion ;
    np:hasProvenance dgn-np:NP267474.RA7sChAUkLvk3P2E3cYCwFWN3F19Gp3QlnuE4cpyMPoeI130_provenance ;
    np:hasPublicationInfo dgn-np:NP267474.RA7sChAUkLvk3P2E3cYCwFWN3F19Gp3QlnuE4cpyMPoeI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP267474.RA7sChAUkLvk3P2E3cYCwFWN3F19Gp3QlnuE4cpyMPoeI130_assertion a np:Assertion .
  dgn-np:NP267474.RA7sChAUkLvk3P2E3cYCwFWN3F19Gp3QlnuE4cpyMPoeI130_provenance a np:Provenance .
  dgn-np:NP267474.RA7sChAUkLvk3P2E3cYCwFWN3F19Gp3QlnuE4cpyMPoeI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP267474.RA7sChAUkLvk3P2E3cYCwFWN3F19Gp3QlnuE4cpyMPoeI130_assertion {
  miriam-gene:2263 a ncit:C16612 .
  lld:C0006142 a ncit:C7057 .
  dgn-gda:DGNab6ce15bd752b4ed8fcdba6aaeff2657 sio:SIO_000628 miriam-gene:2263 , lld:C0006142 ;
    a sio:SIO_001121 .
}
dgn-np:NP267474.RA7sChAUkLvk3P2E3cYCwFWN3F19Gp3QlnuE4cpyMPoeI130_provenance {
  dgn-np:NP267474.RA7sChAUkLvk3P2E3cYCwFWN3F19Gp3QlnuE4cpyMPoeI130_assertion dcterms:description "[Our results demonstrate that the association of SNPs in FGFR2 with BC risk extends to women of African American ethnicity, and illustrate the utility of combining association analysis in datasets of diverse ethnic groups with functional experiments to identify disease susceptibility variants.]. 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:19223389 ;
    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:NP267474.RA7sChAUkLvk3P2E3cYCwFWN3F19Gp3QlnuE4cpyMPoeI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:29+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" .
}