@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP263098.RAAHlO5sVUWyLIL-r-PEq9wWOibbShE3U1TOnEgZWfLfU> .
@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:NP263098.RAAHlO5sVUWyLIL-r-PEq9wWOibbShE3U1TOnEgZWfLfU130_head {
  this: np:hasAssertion dgn-np:NP263098.RAAHlO5sVUWyLIL-r-PEq9wWOibbShE3U1TOnEgZWfLfU130_assertion;
    np:hasProvenance dgn-np:NP263098.RAAHlO5sVUWyLIL-r-PEq9wWOibbShE3U1TOnEgZWfLfU130_provenance;
    np:hasPublicationInfo dgn-np:NP263098.RAAHlO5sVUWyLIL-r-PEq9wWOibbShE3U1TOnEgZWfLfU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP263098.RAAHlO5sVUWyLIL-r-PEq9wWOibbShE3U1TOnEgZWfLfU130_assertion a np:Assertion .
  
  dgn-np:NP263098.RAAHlO5sVUWyLIL-r-PEq9wWOibbShE3U1TOnEgZWfLfU130_provenance a np:Provenance .
  
  dgn-np:NP263098.RAAHlO5sVUWyLIL-r-PEq9wWOibbShE3U1TOnEgZWfLfU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP263098.RAAHlO5sVUWyLIL-r-PEq9wWOibbShE3U1TOnEgZWfLfU130_assertion {
  miriam-gene:8926 a ncit:C16612 .
  
  lld:C0032897 a ncit:C7057 .
  
  dgn-gda:DGN945df16c8f82045c5469103c63d97382 sio:SIO_000628 miriam-gene:8926, lld:C0032897;
    a sio:SIO_001121 .
}

dgn-np:NP263098.RAAHlO5sVUWyLIL-r-PEq9wWOibbShE3U1TOnEgZWfLfU130_provenance {
  dgn-np:NP263098.RAAHlO5sVUWyLIL-r-PEq9wWOibbShE3U1TOnEgZWfLfU130_assertion dcterms:description
      "[Nine probands with a firm clinical diagnosis of PWS but who had neither a typical deletion in the PWS region nor UPD(15)mat were investigated for inactivating mutations in 11 genes located in the PWS region, including SNURF and SNRPN, which are associated with the imprinting centre.]. 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:17262171;
    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:NP263098.RAAHlO5sVUWyLIL-r-PEq9wWOibbShE3U1TOnEgZWfLfU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:27+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>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}