@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP701749.RAiMqv9lOwbfDXUGgLhr22aJZynaKktRRSgbsyhNx8Whs> .
@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:NP701749.RAiMqv9lOwbfDXUGgLhr22aJZynaKktRRSgbsyhNx8Whs130_head {
  this: np:hasAssertion dgn-np:NP701749.RAiMqv9lOwbfDXUGgLhr22aJZynaKktRRSgbsyhNx8Whs130_assertion;
    np:hasProvenance dgn-np:NP701749.RAiMqv9lOwbfDXUGgLhr22aJZynaKktRRSgbsyhNx8Whs130_provenance;
    np:hasPublicationInfo dgn-np:NP701749.RAiMqv9lOwbfDXUGgLhr22aJZynaKktRRSgbsyhNx8Whs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP701749.RAiMqv9lOwbfDXUGgLhr22aJZynaKktRRSgbsyhNx8Whs130_assertion a np:Assertion .
  
  dgn-np:NP701749.RAiMqv9lOwbfDXUGgLhr22aJZynaKktRRSgbsyhNx8Whs130_provenance a np:Provenance .
  
  dgn-np:NP701749.RAiMqv9lOwbfDXUGgLhr22aJZynaKktRRSgbsyhNx8Whs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP701749.RAiMqv9lOwbfDXUGgLhr22aJZynaKktRRSgbsyhNx8Whs130_assertion {
  miriam-gene:4163 a ncit:C16612 .
  
  lld:C0678222 a ncit:C7057 .
  
  dgn-gda:DGN761619ea8daaaf5daaf96f3d8348e90f sio:SIO_000628 miriam-gene:4163, lld:C0678222;
    a sio:SIO_001121 .
}

dgn-np:NP701749.RAiMqv9lOwbfDXUGgLhr22aJZynaKktRRSgbsyhNx8Whs130_provenance {
  dgn-np:NP701749.RAiMqv9lOwbfDXUGgLhr22aJZynaKktRRSgbsyhNx8Whs130_assertion dcterms:description
      "[In the present study we analyzed the association of genotype and haplotype status of two single nucleotide polymorphisms (SNPs), rs2229992 and rs11283943, in the APC and MCC genes, respectively, with an increased risk of breast carcinogenesis in a breast cancer and control population from eastern India.]. 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:21279955;
    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:NP701749.RAiMqv9lOwbfDXUGgLhr22aJZynaKktRRSgbsyhNx8Whs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:06+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}