@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP422937.RAvorcW1fdPfzhi-AvX-6IIRHVhfQa3lpfzKH5dSw-870> .
@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:NP422937.RAvorcW1fdPfzhi-AvX-6IIRHVhfQa3lpfzKH5dSw-870130_head {
  this: np:hasAssertion dgn-np:NP422937.RAvorcW1fdPfzhi-AvX-6IIRHVhfQa3lpfzKH5dSw-870130_assertion;
    np:hasProvenance dgn-np:NP422937.RAvorcW1fdPfzhi-AvX-6IIRHVhfQa3lpfzKH5dSw-870130_provenance;
    np:hasPublicationInfo dgn-np:NP422937.RAvorcW1fdPfzhi-AvX-6IIRHVhfQa3lpfzKH5dSw-870130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP422937.RAvorcW1fdPfzhi-AvX-6IIRHVhfQa3lpfzKH5dSw-870130_assertion a np:Assertion .
  
  dgn-np:NP422937.RAvorcW1fdPfzhi-AvX-6IIRHVhfQa3lpfzKH5dSw-870130_provenance a np:Provenance .
  
  dgn-np:NP422937.RAvorcW1fdPfzhi-AvX-6IIRHVhfQa3lpfzKH5dSw-870130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP422937.RAvorcW1fdPfzhi-AvX-6IIRHVhfQa3lpfzKH5dSw-870130_assertion {
  miriam-gene:3133 a ncit:C16612 .
  
  lld:C0036421 a ncit:C7057 .
  
  dgn-gda:DGNa50841d44e457424cc308523fb06a846 sio:SIO_000628 miriam-gene:3133, lld:C0036421;
    a sio:SIO_001121 .
}

dgn-np:NP422937.RAvorcW1fdPfzhi-AvX-6IIRHVhfQa3lpfzKH5dSw-870130_provenance {
  dgn-np:NP422937.RAvorcW1fdPfzhi-AvX-6IIRHVhfQa3lpfzKH5dSw-870130_assertion dcterms:description
      "[Currently it may be stated that the MHC associations in scleroderma support the classification of disease subsets, but in no ethnic group is the overall association strong enough for clinical use.]. 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:1516246;
    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:NP422937.RAvorcW1fdPfzhi-AvX-6IIRHVhfQa3lpfzKH5dSw-870130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:11+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" .
}