@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP336831.RAqshjsRzLVYz8xv4c-cvFHl7e7fAgcR8mHthjv9bipSs> .
@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:NP336831.RAqshjsRzLVYz8xv4c-cvFHl7e7fAgcR8mHthjv9bipSs130_head {
  this: np:hasAssertion dgn-np:NP336831.RAqshjsRzLVYz8xv4c-cvFHl7e7fAgcR8mHthjv9bipSs130_assertion;
    np:hasProvenance dgn-np:NP336831.RAqshjsRzLVYz8xv4c-cvFHl7e7fAgcR8mHthjv9bipSs130_provenance;
    np:hasPublicationInfo dgn-np:NP336831.RAqshjsRzLVYz8xv4c-cvFHl7e7fAgcR8mHthjv9bipSs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP336831.RAqshjsRzLVYz8xv4c-cvFHl7e7fAgcR8mHthjv9bipSs130_assertion a np:Assertion .
  
  dgn-np:NP336831.RAqshjsRzLVYz8xv4c-cvFHl7e7fAgcR8mHthjv9bipSs130_provenance a np:Provenance .
  
  dgn-np:NP336831.RAqshjsRzLVYz8xv4c-cvFHl7e7fAgcR8mHthjv9bipSs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP336831.RAqshjsRzLVYz8xv4c-cvFHl7e7fAgcR8mHthjv9bipSs130_assertion {
  miriam-gene:5002 a ncit:C16612 .
  
  lld:C0004903 a ncit:C7057 .
  
  dgn-gda:DGN8962e242152bebcf70a88e9047a3eda2 sio:SIO_000628 miriam-gene:5002, lld:C0004903;
    a sio:SIO_001121 .
}

dgn-np:NP336831.RAqshjsRzLVYz8xv4c-cvFHl7e7fAgcR8mHthjv9bipSs130_provenance {
  dgn-np:NP336831.RAqshjsRzLVYz8xv4c-cvFHl7e7fAgcR8mHthjv9bipSs130_assertion dcterms:description
      "[Although SSCP analysis of 62 WT samples and 10 BWS patients did not result in the identification of any mutations in ORCTL2 or ORCTL2S, it will be important to examine their expression pattern in tumors and BWS patients, since epigenetic alteration at these loci may play a role in the etiology of these diseases.]. 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:9570947;
    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:NP336831.RAqshjsRzLVYz8xv4c-cvFHl7e7fAgcR8mHthjv9bipSs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:18+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" .
}