@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP160903.RAp_gkMXsXKMYbpSiiXTh5KFQe81hsybc_dPvirlxoKfU> .
@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:NP160903.RAp_gkMXsXKMYbpSiiXTh5KFQe81hsybc_dPvirlxoKfU130_head {
  this: np:hasAssertion dgn-np:NP160903.RAp_gkMXsXKMYbpSiiXTh5KFQe81hsybc_dPvirlxoKfU130_assertion;
    np:hasProvenance dgn-np:NP160903.RAp_gkMXsXKMYbpSiiXTh5KFQe81hsybc_dPvirlxoKfU130_provenance;
    np:hasPublicationInfo dgn-np:NP160903.RAp_gkMXsXKMYbpSiiXTh5KFQe81hsybc_dPvirlxoKfU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP160903.RAp_gkMXsXKMYbpSiiXTh5KFQe81hsybc_dPvirlxoKfU130_assertion a np:Assertion .
  
  dgn-np:NP160903.RAp_gkMXsXKMYbpSiiXTh5KFQe81hsybc_dPvirlxoKfU130_provenance a np:Provenance .
  
  dgn-np:NP160903.RAp_gkMXsXKMYbpSiiXTh5KFQe81hsybc_dPvirlxoKfU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP160903.RAp_gkMXsXKMYbpSiiXTh5KFQe81hsybc_dPvirlxoKfU130_assertion {
  miriam-gene:1490 a ncit:C16612 .
  
  lld:C0036421 a ncit:C7057 .
  
  dgn-gda:DGN2e00217a1ef1522e65e02cc1f881334d sio:SIO_000628 miriam-gene:1490, lld:C0036421;
    a sio:SIO_001121 .
}

dgn-np:NP160903.RAp_gkMXsXKMYbpSiiXTh5KFQe81hsybc_dPvirlxoKfU130_provenance {
  dgn-np:NP160903.RAp_gkMXsXKMYbpSiiXTh5KFQe81hsybc_dPvirlxoKfU130_assertion dcterms:description
      "[These data indicate that there is an overexpression of CTGF in the systemic sclerosis cells, probably due to increased gene transcription, and suggest that the dysregulation of CTGF production is an important factor in fibroblast activation and the excessive deposition of collagen in systemic sclerosis.]. 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:10942593;
    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:NP160903.RAp_gkMXsXKMYbpSiiXTh5KFQe81hsybc_dPvirlxoKfU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:27+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" .
}