@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac> .
@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:NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_head {
  this: np:hasAssertion dgn-np:NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_assertion;
    np:hasProvenance dgn-np:NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_provenance;
    np:hasPublicationInfo dgn-np:NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_assertion a np:Assertion .
  
  dgn-np:NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_provenance a np:Provenance .
  
  dgn-np:NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_assertion {
  miriam-gene:100128922 a ncit:C16612 .
  
  lld:C0581883 a ncit:C7057 .
  
  dgn-gda:DGN619a904fc6851826d8b9709828cc44d9 sio:SIO_000628 miriam-gene:100128922,
      lld:C0581883;
    a sio:SIO_001121 .
}

dgn-np:NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_provenance {
  dgn-np:NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_assertion dcterms:description
      "[Interestingly, mutations of connexin genes have been reported in several human diseases (peripheral neuropathies, cardiovascular and dermatological diseases, hereditary cataract, and deafness) and altered expression of connexins have been associated with tumoral progression.]. 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:16677845;
    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:NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:12+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" .
}