@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP785316.RARvyGIEp8MFxYk6HRSI-pEstF9yn6vuZHgJpipxNJzww> .
@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:NP785316.RARvyGIEp8MFxYk6HRSI-pEstF9yn6vuZHgJpipxNJzww130_head {
  this: np:hasAssertion dgn-np:NP785316.RARvyGIEp8MFxYk6HRSI-pEstF9yn6vuZHgJpipxNJzww130_assertion;
    np:hasProvenance dgn-np:NP785316.RARvyGIEp8MFxYk6HRSI-pEstF9yn6vuZHgJpipxNJzww130_provenance;
    np:hasPublicationInfo dgn-np:NP785316.RARvyGIEp8MFxYk6HRSI-pEstF9yn6vuZHgJpipxNJzww130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP785316.RARvyGIEp8MFxYk6HRSI-pEstF9yn6vuZHgJpipxNJzww130_assertion a np:Assertion .
  
  dgn-np:NP785316.RARvyGIEp8MFxYk6HRSI-pEstF9yn6vuZHgJpipxNJzww130_provenance a np:Provenance .
  
  dgn-np:NP785316.RARvyGIEp8MFxYk6HRSI-pEstF9yn6vuZHgJpipxNJzww130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP785316.RARvyGIEp8MFxYk6HRSI-pEstF9yn6vuZHgJpipxNJzww130_assertion {
  miriam-gene:112744 a ncit:C16612 .
  
  lld:C0004364 a ncit:C7057 .
  
  dgn-gda:DGN00ff5cae758ea185aaf8cd4603e37531 sio:SIO_000628 miriam-gene:112744, lld:C0004364;
    a sio:SIO_001121 .
}

dgn-np:NP785316.RARvyGIEp8MFxYk6HRSI-pEstF9yn6vuZHgJpipxNJzww130_provenance {
  dgn-np:NP785316.RARvyGIEp8MFxYk6HRSI-pEstF9yn6vuZHgJpipxNJzww130_assertion dcterms:description
      "[Among IL-17 families, IL-17A and IL-17F share amino acid sequence similarity and bind to IL-17R type A. IL-17 signaling is implicated in the pathogenesis of various autoimmune diseases, but its role in the regulatory mechanism of extracellular matrix expression and its contribution to the phenotype of systemic sclerosis (SSc) both remain to be elucidated.]. 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:22403442;
    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:NP785316.RARvyGIEp8MFxYk6HRSI-pEstF9yn6vuZHgJpipxNJzww130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:55+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" .
}