@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP369457.RA4Ep9H3_JT3wpy5Gy9DHSX7qifv7ncvnHfbPBHwgIWZE> .
@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:NP369457.RA4Ep9H3_JT3wpy5Gy9DHSX7qifv7ncvnHfbPBHwgIWZE130_head {
  this: np:hasAssertion dgn-np:NP369457.RA4Ep9H3_JT3wpy5Gy9DHSX7qifv7ncvnHfbPBHwgIWZE130_assertion ;
    np:hasProvenance dgn-np:NP369457.RA4Ep9H3_JT3wpy5Gy9DHSX7qifv7ncvnHfbPBHwgIWZE130_provenance ;
    np:hasPublicationInfo dgn-np:NP369457.RA4Ep9H3_JT3wpy5Gy9DHSX7qifv7ncvnHfbPBHwgIWZE130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP369457.RA4Ep9H3_JT3wpy5Gy9DHSX7qifv7ncvnHfbPBHwgIWZE130_provenance a np:Provenance .
  dgn-np:NP369457.RA4Ep9H3_JT3wpy5Gy9DHSX7qifv7ncvnHfbPBHwgIWZE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP369457.RA4Ep9H3_JT3wpy5Gy9DHSX7qifv7ncvnHfbPBHwgIWZE130_assertion {
  miriam-gene:28 a ncit:C16612 .
  lld:C0006826 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP369457.RA4Ep9H3_JT3wpy5Gy9DHSX7qifv7ncvnHfbPBHwgIWZE130_provenance {
  dgn-np:NP369457.RA4Ep9H3_JT3wpy5Gy9DHSX7qifv7ncvnHfbPBHwgIWZE130_assertion dcterms:description "[We compared familial and sporadic breast cancer cases with respect to ABO blood group distribution and the risk of bilateral disease, using the data from the Icelandic Cancer Registry which contains genealogical information for about 30% of the breast cancer cases diagnosed in Iceland since 1911.]. 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:3170024 ;
    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:NP369457.RA4Ep9H3_JT3wpy5Gy9DHSX7qifv7ncvnHfbPBHwgIWZE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:36+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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}