@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP819756.RAf1XTcjMAhnAH50UFh2nqiTELf9c7rreip4djiUXMJuo> .
@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/v4.0.0/void/> .

dgn-np:NP819756.RAf1XTcjMAhnAH50UFh2nqiTELf9c7rreip4djiUXMJuo130_head {
  this: np:hasAssertion dgn-np:NP819756.RAf1XTcjMAhnAH50UFh2nqiTELf9c7rreip4djiUXMJuo130_assertion;
    np:hasProvenance dgn-np:NP819756.RAf1XTcjMAhnAH50UFh2nqiTELf9c7rreip4djiUXMJuo130_provenance;
    np:hasPublicationInfo dgn-np:NP819756.RAf1XTcjMAhnAH50UFh2nqiTELf9c7rreip4djiUXMJuo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP819756.RAf1XTcjMAhnAH50UFh2nqiTELf9c7rreip4djiUXMJuo130_assertion a np:Assertion .
  
  dgn-np:NP819756.RAf1XTcjMAhnAH50UFh2nqiTELf9c7rreip4djiUXMJuo130_provenance a np:Provenance .
  
  dgn-np:NP819756.RAf1XTcjMAhnAH50UFh2nqiTELf9c7rreip4djiUXMJuo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP819756.RAf1XTcjMAhnAH50UFh2nqiTELf9c7rreip4djiUXMJuo130_assertion {
  miriam-gene:1543 a ncit:C16612 .
  
  lld:C0023267 a ncit:C7057 .
  
  dgn-gda:DGN96bf6a9ed003a8634e71abda19a0d335 sio:SIO_000628 miriam-gene:1543, lld:C0023267;
    a sio:SIO_001122 .
}

dgn-np:NP819756.RAf1XTcjMAhnAH50UFh2nqiTELf9c7rreip4djiUXMJuo130_provenance {
  dgn-np:NP819756.RAf1XTcjMAhnAH50UFh2nqiTELf9c7rreip4djiUXMJuo130_assertion dcterms:description
      "[We concluded that the carriage of CYP1A1 Ile462Val AG and CYP1B1 Leu 432Val CC genotypes predict the susceptibility to leiomyoma in Egyptian women and they are likely to contribute in the pathogenesis of leiomyoma.]. 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:20559649;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP819756.RAf1XTcjMAhnAH50UFh2nqiTELf9c7rreip4djiUXMJuo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:56+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}