@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP50674.RAmwxoi40P91pQrFAgmGwdQ5o30v3WmSVQXW8hMxas1oU> .
@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:NP50674.RAmwxoi40P91pQrFAgmGwdQ5o30v3WmSVQXW8hMxas1oU130_head {
  this: np:hasAssertion dgn-np:NP50674.RAmwxoi40P91pQrFAgmGwdQ5o30v3WmSVQXW8hMxas1oU130_assertion;
    np:hasProvenance dgn-np:NP50674.RAmwxoi40P91pQrFAgmGwdQ5o30v3WmSVQXW8hMxas1oU130_provenance;
    np:hasPublicationInfo dgn-np:NP50674.RAmwxoi40P91pQrFAgmGwdQ5o30v3WmSVQXW8hMxas1oU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP50674.RAmwxoi40P91pQrFAgmGwdQ5o30v3WmSVQXW8hMxas1oU130_assertion a np:Assertion .
  
  dgn-np:NP50674.RAmwxoi40P91pQrFAgmGwdQ5o30v3WmSVQXW8hMxas1oU130_provenance a np:Provenance .
  
  dgn-np:NP50674.RAmwxoi40P91pQrFAgmGwdQ5o30v3WmSVQXW8hMxas1oU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP50674.RAmwxoi40P91pQrFAgmGwdQ5o30v3WmSVQXW8hMxas1oU130_assertion {
  miriam-gene:7040 a ncit:C16612 .
  
  lld:C0036421 a ncit:C7057 .
  
  dgn-gda:DGNff7481b8085ecc59f6f8ad1f46bd67ac sio:SIO_000628 miriam-gene:7040, lld:C0036421;
    a sio:SIO_001122 .
}

dgn-np:NP50674.RAmwxoi40P91pQrFAgmGwdQ5o30v3WmSVQXW8hMxas1oU130_provenance {
  dgn-np:NP50674.RAmwxoi40P91pQrFAgmGwdQ5o30v3WmSVQXW8hMxas1oU130_assertion dcterms:description
      "[ These results suggest that patients with SSc are genetically predisposed to high TGFbeta1 production. These polymorphisms do not, however, explain the difference in the clinical phenotypes of limited and diffuse SSc.]. 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:12117671;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP50674.RAmwxoi40P91pQrFAgmGwdQ5o30v3WmSVQXW8hMxas1oU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:23+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" .
}