@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1208466.RABCSFtXENBD32VFP2utlisDORkg56i8iUoMbo0t3KCZo> .
@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:NP1208466.RABCSFtXENBD32VFP2utlisDORkg56i8iUoMbo0t3KCZo130_head {
  this: np:hasAssertion dgn-np:NP1208466.RABCSFtXENBD32VFP2utlisDORkg56i8iUoMbo0t3KCZo130_assertion;
    np:hasProvenance dgn-np:NP1208466.RABCSFtXENBD32VFP2utlisDORkg56i8iUoMbo0t3KCZo130_provenance;
    np:hasPublicationInfo dgn-np:NP1208466.RABCSFtXENBD32VFP2utlisDORkg56i8iUoMbo0t3KCZo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1208466.RABCSFtXENBD32VFP2utlisDORkg56i8iUoMbo0t3KCZo130_assertion a np:Assertion .
  
  dgn-np:NP1208466.RABCSFtXENBD32VFP2utlisDORkg56i8iUoMbo0t3KCZo130_provenance a np:Provenance .
  
  dgn-np:NP1208466.RABCSFtXENBD32VFP2utlisDORkg56i8iUoMbo0t3KCZo130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1208466.RABCSFtXENBD32VFP2utlisDORkg56i8iUoMbo0t3KCZo130_assertion {
  miriam-gene:2705 a ncit:C16612 .
  
  lld:C0338656 a ncit:C7057 .
  
  dgn-gda:DGN578b8bbe27fb256b4b9b510c24f92a24 sio:SIO_000628 miriam-gene:2705, lld:C0338656;
    a sio:SIO_001121 .
}

dgn-np:NP1208466.RABCSFtXENBD32VFP2utlisDORkg56i8iUoMbo0t3KCZo130_provenance {
  dgn-np:NP1208466.RABCSFtXENBD32VFP2utlisDORkg56i8iUoMbo0t3KCZo130_assertion dcterms:description
      "[Because increasing cortical abnormalities correlate with disease progression and cognitive dysfunction, we examined the expression of oligodendrocytic connexin32 (Cx32) and Cx47 and their astrocytic partners Cx30 and Cx43 in cortical lesions and normal-appearing gray matter (NAGM) in MS patients.]. 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:25101702;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1208466.RABCSFtXENBD32VFP2utlisDORkg56i8iUoMbo0t3KCZo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:53+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" .
}