@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP600906.RARGiOZ2fHg4Ge3C6zyMsZ4MbkiqN10kdd6k7oobEzylY> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP600906.RARGiOZ2fHg4Ge3C6zyMsZ4MbkiqN10kdd6k7oobEzylY130_head {
  this: np:hasAssertion dgn-np:NP600906.RARGiOZ2fHg4Ge3C6zyMsZ4MbkiqN10kdd6k7oobEzylY130_assertion;
    np:hasProvenance dgn-np:NP600906.RARGiOZ2fHg4Ge3C6zyMsZ4MbkiqN10kdd6k7oobEzylY130_provenance;
    np:hasPublicationInfo dgn-np:NP600906.RARGiOZ2fHg4Ge3C6zyMsZ4MbkiqN10kdd6k7oobEzylY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP600906.RARGiOZ2fHg4Ge3C6zyMsZ4MbkiqN10kdd6k7oobEzylY130_assertion a np:Assertion .
  
  dgn-np:NP600906.RARGiOZ2fHg4Ge3C6zyMsZ4MbkiqN10kdd6k7oobEzylY130_provenance a np:Provenance .
  
  dgn-np:NP600906.RARGiOZ2fHg4Ge3C6zyMsZ4MbkiqN10kdd6k7oobEzylY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP600906.RARGiOZ2fHg4Ge3C6zyMsZ4MbkiqN10kdd6k7oobEzylY130_assertion {
  miriam-gene:4926 a ncit:C16612 .
  
  lld:C0678222 a ncit:C7057 .
  
  dgn-gda:DGNb70b7b833e3065a8cc52602ee6f8131e sio:SIO_000628 miriam-gene:4926, lld:C0678222;
    a sio:SIO_001122 .
}

dgn-np:NP600906.RARGiOZ2fHg4Ge3C6zyMsZ4MbkiqN10kdd6k7oobEzylY130_provenance {
  dgn-np:NP600906.RARGiOZ2fHg4Ge3C6zyMsZ4MbkiqN10kdd6k7oobEzylY130_assertion dcterms:description
      "[Although the potential functional relevance of the A794G variation requires further biological validation, we conclude that variations in the NuMA gene are likely responsible for the observed increased breast cancer risk.]. 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:15684076;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP600906.RARGiOZ2fHg4Ge3C6zyMsZ4MbkiqN10kdd6k7oobEzylY130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:39+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}