@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP589425.RAipsU9rmHyzEb8FL9IsFaKvJQeaAvOehUAONeETHSdhg> .
@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:NP589425.RAipsU9rmHyzEb8FL9IsFaKvJQeaAvOehUAONeETHSdhg130_head {
  this: np:hasAssertion dgn-np:NP589425.RAipsU9rmHyzEb8FL9IsFaKvJQeaAvOehUAONeETHSdhg130_assertion;
    np:hasProvenance dgn-np:NP589425.RAipsU9rmHyzEb8FL9IsFaKvJQeaAvOehUAONeETHSdhg130_provenance;
    np:hasPublicationInfo dgn-np:NP589425.RAipsU9rmHyzEb8FL9IsFaKvJQeaAvOehUAONeETHSdhg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP589425.RAipsU9rmHyzEb8FL9IsFaKvJQeaAvOehUAONeETHSdhg130_assertion a np:Assertion .
  
  dgn-np:NP589425.RAipsU9rmHyzEb8FL9IsFaKvJQeaAvOehUAONeETHSdhg130_provenance a np:Provenance .
  
  dgn-np:NP589425.RAipsU9rmHyzEb8FL9IsFaKvJQeaAvOehUAONeETHSdhg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP589425.RAipsU9rmHyzEb8FL9IsFaKvJQeaAvOehUAONeETHSdhg130_assertion {
  miriam-gene:7389 a ncit:C16612 .
  
  lld:C1297882 a ncit:C7057 .
  
  dgn-gda:DGN100981f83ac373537c6a4573b3ef76cb sio:SIO_000628 miriam-gene:7389, lld:C1297882;
    a sio:SIO_001121 .
}

dgn-np:NP589425.RAipsU9rmHyzEb8FL9IsFaKvJQeaAvOehUAONeETHSdhg130_provenance {
  dgn-np:NP589425.RAipsU9rmHyzEb8FL9IsFaKvJQeaAvOehUAONeETHSdhg130_assertion dcterms:description
      "[Our study, in conjunction with a prior study of UPD 14 and partial trisomy 14 cases, and what is known of imprinting in regions of mouse chromosomes homologous to human chromosome 14, leads us to conclude that 14q23-q32 is likely an area where imprinted genes may reside.]. 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:10951461;
    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:NP589425.RAipsU9rmHyzEb8FL9IsFaKvJQeaAvOehUAONeETHSdhg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:54+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" .
}