@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP161178.RARSh1tvi-LAWIuiwMCUQ1Vg03iRH8_JaS0VwLdUDNzVk> .
@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:NP161178.RARSh1tvi-LAWIuiwMCUQ1Vg03iRH8_JaS0VwLdUDNzVk130_head {
  this: np:hasAssertion dgn-np:NP161178.RARSh1tvi-LAWIuiwMCUQ1Vg03iRH8_JaS0VwLdUDNzVk130_assertion;
    np:hasProvenance dgn-np:NP161178.RARSh1tvi-LAWIuiwMCUQ1Vg03iRH8_JaS0VwLdUDNzVk130_provenance;
    np:hasPublicationInfo dgn-np:NP161178.RARSh1tvi-LAWIuiwMCUQ1Vg03iRH8_JaS0VwLdUDNzVk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP161178.RARSh1tvi-LAWIuiwMCUQ1Vg03iRH8_JaS0VwLdUDNzVk130_assertion a np:Assertion .
  
  dgn-np:NP161178.RARSh1tvi-LAWIuiwMCUQ1Vg03iRH8_JaS0VwLdUDNzVk130_provenance a np:Provenance .
  
  dgn-np:NP161178.RARSh1tvi-LAWIuiwMCUQ1Vg03iRH8_JaS0VwLdUDNzVk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP161178.RARSh1tvi-LAWIuiwMCUQ1Vg03iRH8_JaS0VwLdUDNzVk130_assertion {
  miriam-gene:871 a ncit:C16612 .
  
  lld:C0022548 a ncit:C7057 .
  
  dgn-gda:DGNd27e3a3450027a4c98f4638f33086ca8 sio:SIO_000628 miriam-gene:871, lld:C0022548;
    a sio:SIO_001121 .
}

dgn-np:NP161178.RARSh1tvi-LAWIuiwMCUQ1Vg03iRH8_JaS0VwLdUDNzVk130_provenance {
  dgn-np:NP161178.RARSh1tvi-LAWIuiwMCUQ1Vg03iRH8_JaS0VwLdUDNzVk130_assertion dcterms:description
      "[Combining the results of our previous in vitro experiment results, we suggest that overexpression of HSP47 in keloid fibroblast cells could induce excessive collagen accumulation by enhancing collagen synthesis, which not only presents a possible mechanism of keloid formation, but also offers a therapeutic potential of RNA interference to HSP47 for the treatment of keloids and other fibroproliferative disorders.]. 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:22295344;
    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:NP161178.RARSh1tvi-LAWIuiwMCUQ1Vg03iRH8_JaS0VwLdUDNzVk130_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" .
}