@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP45006.RATPkCZIkPu9hihC4WHRE84-0WVNGlxkFP1WH62ujeQbw> .
@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:NP45006.RATPkCZIkPu9hihC4WHRE84-0WVNGlxkFP1WH62ujeQbw130_head {
  this: np:hasAssertion dgn-np:NP45006.RATPkCZIkPu9hihC4WHRE84-0WVNGlxkFP1WH62ujeQbw130_assertion ;
    np:hasProvenance dgn-np:NP45006.RATPkCZIkPu9hihC4WHRE84-0WVNGlxkFP1WH62ujeQbw130_provenance ;
    np:hasPublicationInfo dgn-np:NP45006.RATPkCZIkPu9hihC4WHRE84-0WVNGlxkFP1WH62ujeQbw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP45006.RATPkCZIkPu9hihC4WHRE84-0WVNGlxkFP1WH62ujeQbw130_assertion a np:Assertion .
  dgn-np:NP45006.RATPkCZIkPu9hihC4WHRE84-0WVNGlxkFP1WH62ujeQbw130_provenance a np:Provenance .
  dgn-np:NP45006.RATPkCZIkPu9hihC4WHRE84-0WVNGlxkFP1WH62ujeQbw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP45006.RATPkCZIkPu9hihC4WHRE84-0WVNGlxkFP1WH62ujeQbw130_assertion {
  miriam-gene:2064 a ncit:C16612 .
  lld:C0005684 a ncit:C7057 .
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    a sio:SIO_001122 .
}
dgn-np:NP45006.RATPkCZIkPu9hihC4WHRE84-0WVNGlxkFP1WH62ujeQbw130_provenance {
  dgn-np:NP45006.RATPkCZIkPu9hihC4WHRE84-0WVNGlxkFP1WH62ujeQbw130_assertion dcterms:description "[These data suggest that this SNP has variable frequency in different ethnic groups. In addition, intraracial differences in allele frequency were seen. The presence of the Val allele in the African-American population, but not in the African population is consistent with the genetic mixing, which has been identified through historical and molecular analysis. However, the presence of many first-generation immigrant populations in the United States provides warning for the overinterpretation of results from any one ethnic group. Therefore, the usefulness of the HER2 SNP in the determination of risk, prognosis, and treatment response of breast cancer will be dramatically different between ethnic populations.]. 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:11106692 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP45006.RATPkCZIkPu9hihC4WHRE84-0WVNGlxkFP1WH62ujeQbw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:20+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> ;
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