@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP195593.RAQ9ylSbY3I1rTfrUHNbOF3-umLtUEDYDy-rYPrH-2mpI> .
@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:NP195593.RAQ9ylSbY3I1rTfrUHNbOF3-umLtUEDYDy-rYPrH-2mpI130_head {
  this: np:hasAssertion dgn-np:NP195593.RAQ9ylSbY3I1rTfrUHNbOF3-umLtUEDYDy-rYPrH-2mpI130_assertion;
    np:hasProvenance dgn-np:NP195593.RAQ9ylSbY3I1rTfrUHNbOF3-umLtUEDYDy-rYPrH-2mpI130_provenance;
    np:hasPublicationInfo dgn-np:NP195593.RAQ9ylSbY3I1rTfrUHNbOF3-umLtUEDYDy-rYPrH-2mpI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP195593.RAQ9ylSbY3I1rTfrUHNbOF3-umLtUEDYDy-rYPrH-2mpI130_assertion a np:Assertion .
  
  dgn-np:NP195593.RAQ9ylSbY3I1rTfrUHNbOF3-umLtUEDYDy-rYPrH-2mpI130_provenance a np:Provenance .
  
  dgn-np:NP195593.RAQ9ylSbY3I1rTfrUHNbOF3-umLtUEDYDy-rYPrH-2mpI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP195593.RAQ9ylSbY3I1rTfrUHNbOF3-umLtUEDYDy-rYPrH-2mpI130_assertion {
  miriam-gene:3133 a ncit:C16612 .
  
  lld:C0018133 a ncit:C7057 .
  
  dgn-gda:DGN959319502c5645c002401e4d79dc2558 sio:SIO_000628 miriam-gene:3133, lld:C0018133;
    a sio:SIO_001121 .
}

dgn-np:NP195593.RAQ9ylSbY3I1rTfrUHNbOF3-umLtUEDYDy-rYPrH-2mpI130_provenance {
  dgn-np:NP195593.RAQ9ylSbY3I1rTfrUHNbOF3-umLtUEDYDy-rYPrH-2mpI130_assertion dcterms:description
      "[Although disparity at loci within the MHC is the most important risk factor for the development of severe GVHD, disparity at loci outside the MHC that encode minor histocompatibility (H) antigens can elicit GVHD and GVL activity in donor/recipient pairs who are otherwise genetically identical across the MHC.]. 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:22859606;
    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:NP195593.RAQ9ylSbY3I1rTfrUHNbOF3-umLtUEDYDy-rYPrH-2mpI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:47+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" .
}