@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP574198.RAnreLSXhB2-uOcqw5uVp6p_BYtIhPcqWA3rjU9AwGR8c> .
@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:NP574198.RAnreLSXhB2-uOcqw5uVp6p_BYtIhPcqWA3rjU9AwGR8c130_head {
  this: np:hasAssertion dgn-np:NP574198.RAnreLSXhB2-uOcqw5uVp6p_BYtIhPcqWA3rjU9AwGR8c130_assertion;
    np:hasProvenance dgn-np:NP574198.RAnreLSXhB2-uOcqw5uVp6p_BYtIhPcqWA3rjU9AwGR8c130_provenance;
    np:hasPublicationInfo dgn-np:NP574198.RAnreLSXhB2-uOcqw5uVp6p_BYtIhPcqWA3rjU9AwGR8c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP574198.RAnreLSXhB2-uOcqw5uVp6p_BYtIhPcqWA3rjU9AwGR8c130_assertion a np:Assertion .
  
  dgn-np:NP574198.RAnreLSXhB2-uOcqw5uVp6p_BYtIhPcqWA3rjU9AwGR8c130_provenance a np:Provenance .
  
  dgn-np:NP574198.RAnreLSXhB2-uOcqw5uVp6p_BYtIhPcqWA3rjU9AwGR8c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP574198.RAnreLSXhB2-uOcqw5uVp6p_BYtIhPcqWA3rjU9AwGR8c130_assertion {
  miriam-gene:6638 a ncit:C16612 .
  
  lld:C0032897 a ncit:C7057 .
  
  dgn-gda:DGNd9a7e7a3201ca9ec11e6a276162ac8aa sio:SIO_000628 miriam-gene:6638, lld:C0032897;
    a sio:SIO_001121 .
}

dgn-np:NP574198.RAnreLSXhB2-uOcqw5uVp6p_BYtIhPcqWA3rjU9AwGR8c130_provenance {
  dgn-np:NP574198.RAnreLSXhB2-uOcqw5uVp6p_BYtIhPcqWA3rjU9AwGR8c130_assertion dcterms:description
      "[In cases of Prader-Willi syndrome (PWS), a total of 24 patients with PWS, as well as 205 control individuals from the general population, were analyzed by use of multiplex quantitative PCR to amplify the FGFR2 gene, the KRIT1 gene, and the SNRPN gene simultaneously.]. 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:17040959;
    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:NP574198.RAnreLSXhB2-uOcqw5uVp6p_BYtIhPcqWA3rjU9AwGR8c130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:05+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" .
}