@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP50676.RAO8N6wSjogpGqv5CHkPELAPL9fGP5LL-WRUnDStUh83s> .
@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:NP50676.RAO8N6wSjogpGqv5CHkPELAPL9fGP5LL-WRUnDStUh83s130_head {
  this: np:hasAssertion dgn-np:NP50676.RAO8N6wSjogpGqv5CHkPELAPL9fGP5LL-WRUnDStUh83s130_assertion;
    np:hasProvenance dgn-np:NP50676.RAO8N6wSjogpGqv5CHkPELAPL9fGP5LL-WRUnDStUh83s130_provenance;
    np:hasPublicationInfo dgn-np:NP50676.RAO8N6wSjogpGqv5CHkPELAPL9fGP5LL-WRUnDStUh83s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP50676.RAO8N6wSjogpGqv5CHkPELAPL9fGP5LL-WRUnDStUh83s130_assertion a np:Assertion .
  
  dgn-np:NP50676.RAO8N6wSjogpGqv5CHkPELAPL9fGP5LL-WRUnDStUh83s130_provenance a np:Provenance .
  
  dgn-np:NP50676.RAO8N6wSjogpGqv5CHkPELAPL9fGP5LL-WRUnDStUh83s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP50676.RAO8N6wSjogpGqv5CHkPELAPL9fGP5LL-WRUnDStUh83s130_assertion {
  miriam-gene:7040 a ncit:C16612 .
  
  lld:C0036421 a ncit:C7057 .
  
  dgn-gda:DGN11bb86af6bee81475f187c645be9361c sio:SIO_000628 miriam-gene:7040, lld:C0036421;
    a sio:SIO_001122 .
}

dgn-np:NP50676.RAO8N6wSjogpGqv5CHkPELAPL9fGP5LL-WRUnDStUh83s130_provenance {
  dgn-np:NP50676.RAO8N6wSjogpGqv5CHkPELAPL9fGP5LL-WRUnDStUh83s130_assertion dcterms:description
      "[ The results of these preliminary analyses suggest that genetic anomalies of the TGFbeta1 and PDGF gene families are not likely to explain the dysregulation seen in SSc or to account for the susceptibility to SSc in this population.]. 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:10817561;
    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:NP50676.RAO8N6wSjogpGqv5CHkPELAPL9fGP5LL-WRUnDStUh83s130_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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}