@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP72275.RAWqD_2FDfNwbHsz_ivXMac1arVq_NeZ7sY8aKAzTfoBc> .
@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:NP72275.RAWqD_2FDfNwbHsz_ivXMac1arVq_NeZ7sY8aKAzTfoBc130_head {
  this: np:hasAssertion dgn-np:NP72275.RAWqD_2FDfNwbHsz_ivXMac1arVq_NeZ7sY8aKAzTfoBc130_assertion;
    np:hasProvenance dgn-np:NP72275.RAWqD_2FDfNwbHsz_ivXMac1arVq_NeZ7sY8aKAzTfoBc130_provenance;
    np:hasPublicationInfo dgn-np:NP72275.RAWqD_2FDfNwbHsz_ivXMac1arVq_NeZ7sY8aKAzTfoBc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP72275.RAWqD_2FDfNwbHsz_ivXMac1arVq_NeZ7sY8aKAzTfoBc130_assertion a np:Assertion .
  
  dgn-np:NP72275.RAWqD_2FDfNwbHsz_ivXMac1arVq_NeZ7sY8aKAzTfoBc130_provenance a np:Provenance .
  
  dgn-np:NP72275.RAWqD_2FDfNwbHsz_ivXMac1arVq_NeZ7sY8aKAzTfoBc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP72275.RAWqD_2FDfNwbHsz_ivXMac1arVq_NeZ7sY8aKAzTfoBc130_assertion {
  miriam-gene:3557 a ncit:C16612 .
  
  lld:C1956346 a ncit:C7057 .
  
  dgn-gda:DGNa1526dd551703e9223af1a125610f21f sio:SIO_000628 miriam-gene:3557, lld:C1956346;
    a sio:SIO_001122 .
}

dgn-np:NP72275.RAWqD_2FDfNwbHsz_ivXMac1arVq_NeZ7sY8aKAzTfoBc130_provenance {
  dgn-np:NP72275.RAWqD_2FDfNwbHsz_ivXMac1arVq_NeZ7sY8aKAzTfoBc130_assertion dcterms:description
      "[Despite the multiple hypotheses tested, the robustness of family design to population confoundings and the consistency with previous findings increase the likelihood of true association. Further investigation using larger data sets is needed in order for this to be confirmed. See the related commentary by Keavney: http://www.biomedcentral.com/1741-7015/8/6.]. 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:20070880;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP72275.RAWqD_2FDfNwbHsz_ivXMac1arVq_NeZ7sY8aKAzTfoBc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:35+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" .
}