@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP112754.RANeJcfNWQ2z2MnlTA6o9W_ust65cim5BXIg1Geiz6vxE> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP112754.RANeJcfNWQ2z2MnlTA6o9W_ust65cim5BXIg1Geiz6vxE130_head {
  this: np:hasAssertion dgn-np:NP112754.RANeJcfNWQ2z2MnlTA6o9W_ust65cim5BXIg1Geiz6vxE130_assertion;
    np:hasProvenance dgn-np:NP112754.RANeJcfNWQ2z2MnlTA6o9W_ust65cim5BXIg1Geiz6vxE130_provenance;
    np:hasPublicationInfo dgn-np:NP112754.RANeJcfNWQ2z2MnlTA6o9W_ust65cim5BXIg1Geiz6vxE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP112754.RANeJcfNWQ2z2MnlTA6o9W_ust65cim5BXIg1Geiz6vxE130_assertion a np:Assertion .
  
  dgn-np:NP112754.RANeJcfNWQ2z2MnlTA6o9W_ust65cim5BXIg1Geiz6vxE130_provenance a np:Provenance .
  
  dgn-np:NP112754.RANeJcfNWQ2z2MnlTA6o9W_ust65cim5BXIg1Geiz6vxE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP112754.RANeJcfNWQ2z2MnlTA6o9W_ust65cim5BXIg1Geiz6vxE130_assertion {
  miriam-gene:9467 a ncit:C16612 .
  
  lld:C0006111 a ncit:C7057 .
  
  dgn-gda:DGNeac516c781421acf9dd7f116c870329e sio:SIO_000628 miriam-gene:9467, lld:C0006111;
    a sio:SIO_001122 .
}

dgn-np:NP112754.RANeJcfNWQ2z2MnlTA6o9W_ust65cim5BXIg1Geiz6vxE130_provenance {
  dgn-np:NP112754.RANeJcfNWQ2z2MnlTA6o9W_ust65cim5BXIg1Geiz6vxE130_assertion dcterms:description
      "[Our results suggest that genes associated with clinical neurological disease also have detectable effects on subclinical phenotypes. These hypothesis generating data illustrate the use of an unbiased approach to discover novel pathways that may be involve]. 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:17903297;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP112754.RANeJcfNWQ2z2MnlTA6o9W_ust65cim5BXIg1Geiz6vxE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:42:38+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}