@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP574891.RAAhmYL5u5K2B4j8okH5gqcSRckfyTfXE4rAKjB9KdHCQ> .
@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:NP574891.RAAhmYL5u5K2B4j8okH5gqcSRckfyTfXE4rAKjB9KdHCQ130_head {
  this: np:hasAssertion dgn-np:NP574891.RAAhmYL5u5K2B4j8okH5gqcSRckfyTfXE4rAKjB9KdHCQ130_assertion;
    np:hasProvenance dgn-np:NP574891.RAAhmYL5u5K2B4j8okH5gqcSRckfyTfXE4rAKjB9KdHCQ130_provenance;
    np:hasPublicationInfo dgn-np:NP574891.RAAhmYL5u5K2B4j8okH5gqcSRckfyTfXE4rAKjB9KdHCQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP574891.RAAhmYL5u5K2B4j8okH5gqcSRckfyTfXE4rAKjB9KdHCQ130_assertion a np:Assertion .
  
  dgn-np:NP574891.RAAhmYL5u5K2B4j8okH5gqcSRckfyTfXE4rAKjB9KdHCQ130_provenance a np:Provenance .
  
  dgn-np:NP574891.RAAhmYL5u5K2B4j8okH5gqcSRckfyTfXE4rAKjB9KdHCQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP574891.RAAhmYL5u5K2B4j8okH5gqcSRckfyTfXE4rAKjB9KdHCQ130_assertion {
  miriam-gene:5518 a ncit:C16612 .
  
  lld:C0263214 a ncit:C7057 .
  
  dgn-gda:DGN66fe4e289e5d4b1b3f24df2695f03e1f sio:SIO_000628 miriam-gene:5518, lld:C0263214;
    a sio:SIO_001121 .
}

dgn-np:NP574891.RAAhmYL5u5K2B4j8okH5gqcSRckfyTfXE4rAKjB9KdHCQ130_provenance {
  dgn-np:NP574891.RAAhmYL5u5K2B4j8okH5gqcSRckfyTfXE4rAKjB9KdHCQ130_assertion dcterms:description
      "[The present study was performed to determine the frequency of PPP2R1A mutations in exon 5, which harbors previously reported mutation hot spots, and adjacent exon 6, in 209 ovarian and 56 uterine tumors of various histologic subtypes.]. 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:21435433;
    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:NP574891.RAAhmYL5u5K2B4j8okH5gqcSRckfyTfXE4rAKjB9KdHCQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:46+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" .
}