@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP267240.RAfxG3R8iR45TqlWgv0RZZ2njie7cAxzB-aDmSbVrsQOI> .
@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:NP267240.RAfxG3R8iR45TqlWgv0RZZ2njie7cAxzB-aDmSbVrsQOI130_head {
  this: np:hasAssertion dgn-np:NP267240.RAfxG3R8iR45TqlWgv0RZZ2njie7cAxzB-aDmSbVrsQOI130_assertion ;
    np:hasProvenance dgn-np:NP267240.RAfxG3R8iR45TqlWgv0RZZ2njie7cAxzB-aDmSbVrsQOI130_provenance ;
    np:hasPublicationInfo dgn-np:NP267240.RAfxG3R8iR45TqlWgv0RZZ2njie7cAxzB-aDmSbVrsQOI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP267240.RAfxG3R8iR45TqlWgv0RZZ2njie7cAxzB-aDmSbVrsQOI130_assertion a np:Assertion .
  dgn-np:NP267240.RAfxG3R8iR45TqlWgv0RZZ2njie7cAxzB-aDmSbVrsQOI130_provenance a np:Provenance .
  dgn-np:NP267240.RAfxG3R8iR45TqlWgv0RZZ2njie7cAxzB-aDmSbVrsQOI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP267240.RAfxG3R8iR45TqlWgv0RZZ2njie7cAxzB-aDmSbVrsQOI130_assertion {
  miriam-gene:2263 a ncit:C16612 .
  lld:C0678222 a ncit:C7057 .
  dgn-gda:DGN03ca4dab8d3617509f091d6874d1a2a3 sio:SIO_000628 miriam-gene:2263 , lld:C0678222 ;
    a sio:SIO_001121 .
}
dgn-np:NP267240.RAfxG3R8iR45TqlWgv0RZZ2njie7cAxzB-aDmSbVrsQOI130_provenance {
  dgn-np:NP267240.RAfxG3R8iR45TqlWgv0RZZ2njie7cAxzB-aDmSbVrsQOI130_assertion dcterms:description "[In attempt to investigate whether FGFR2 polymorphisms are associated with a risk of breast cancer in Chinese women of the Han nationality, we genotyped single-nucleotide polymorphisms (SNPs) of seven FGFR2 sites (rs2981582, rs17102287, rs17542768, rs10510097, rs11200012, rs3750817, rs2981578) in 816 women including 388 breast cancer patients and 428 healthy controls via the polymerase chain reaction single-strand conformation polymorphism procedure as well as sequence detection.]. 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:21822685 ;
    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:NP267240.RAfxG3R8iR45TqlWgv0RZZ2njie7cAxzB-aDmSbVrsQOI130_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" .
}