@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP770514.RA76Y0744V_QSV3JycxuVv08RA9SUF_UQaEVsUk3CzHRo> .
@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:NP770514.RA76Y0744V_QSV3JycxuVv08RA9SUF_UQaEVsUk3CzHRo130_head {
  this: np:hasAssertion dgn-np:NP770514.RA76Y0744V_QSV3JycxuVv08RA9SUF_UQaEVsUk3CzHRo130_assertion ;
    np:hasProvenance dgn-np:NP770514.RA76Y0744V_QSV3JycxuVv08RA9SUF_UQaEVsUk3CzHRo130_provenance ;
    np:hasPublicationInfo dgn-np:NP770514.RA76Y0744V_QSV3JycxuVv08RA9SUF_UQaEVsUk3CzHRo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP770514.RA76Y0744V_QSV3JycxuVv08RA9SUF_UQaEVsUk3CzHRo130_assertion a np:Assertion .
  dgn-np:NP770514.RA76Y0744V_QSV3JycxuVv08RA9SUF_UQaEVsUk3CzHRo130_provenance a np:Provenance .
  dgn-np:NP770514.RA76Y0744V_QSV3JycxuVv08RA9SUF_UQaEVsUk3CzHRo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP770514.RA76Y0744V_QSV3JycxuVv08RA9SUF_UQaEVsUk3CzHRo130_assertion {
  miriam-gene:3105 a ncit:C16612 .
  lld:C0026896 a ncit:C7057 .
  dgn-gda:DGNabfa2d7ff8da2b9f8f97ff098ea10158 sio:SIO_000628 miriam-gene:3105 , lld:C0026896 ;
    a sio:SIO_001121 .
}
dgn-np:NP770514.RA76Y0744V_QSV3JycxuVv08RA9SUF_UQaEVsUk3CzHRo130_provenance {
  dgn-np:NP770514.RA76Y0744V_QSV3JycxuVv08RA9SUF_UQaEVsUk3CzHRo130_assertion dcterms:description "[Using the technique of in vitro enzymatic DNA amplification and dot blot hybridization with sequence-specific oligonucleotide (SSO) probes, a study of genetic polymorphism of HLA-DPB1 was performed in 83 unrelated patients with Graves' disease (GD), 48 patients with early onset myasthenia gravis (EOMG) and 100 normal British caucasoid subjects who were also tissue typed for HLA-A, B and DR antigens.]. 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:8061167 ;
    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:NP770514.RA76Y0744V_QSV3JycxuVv08RA9SUF_UQaEVsUk3CzHRo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:46+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" .
}