@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP698423.RATBSzdI30z_P0XCTRv4hl1G6pRB_1wQSlQzJ98Jcnrws> .
@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:NP698423.RATBSzdI30z_P0XCTRv4hl1G6pRB_1wQSlQzJ98Jcnrws130_head {
  this: np:hasAssertion dgn-np:NP698423.RATBSzdI30z_P0XCTRv4hl1G6pRB_1wQSlQzJ98Jcnrws130_assertion ;
    np:hasProvenance dgn-np:NP698423.RATBSzdI30z_P0XCTRv4hl1G6pRB_1wQSlQzJ98Jcnrws130_provenance ;
    np:hasPublicationInfo dgn-np:NP698423.RATBSzdI30z_P0XCTRv4hl1G6pRB_1wQSlQzJ98Jcnrws130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP698423.RATBSzdI30z_P0XCTRv4hl1G6pRB_1wQSlQzJ98Jcnrws130_assertion a np:Assertion .
  dgn-np:NP698423.RATBSzdI30z_P0XCTRv4hl1G6pRB_1wQSlQzJ98Jcnrws130_provenance a np:Provenance .
  dgn-np:NP698423.RATBSzdI30z_P0XCTRv4hl1G6pRB_1wQSlQzJ98Jcnrws130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP698423.RATBSzdI30z_P0XCTRv4hl1G6pRB_1wQSlQzJ98Jcnrws130_assertion {
  miriam-gene:57498 a ncit:C16612 .
  lld:C0018213 a ncit:C7057 .
  dgn-gda:DGN6f56b2bf15a30db67959e20cb1f307db sio:SIO_000628 miriam-gene:57498 , lld:C0018213 ;
    a sio:SIO_001121 .
}
dgn-np:NP698423.RATBSzdI30z_P0XCTRv4hl1G6pRB_1wQSlQzJ98Jcnrws130_provenance {
  dgn-np:NP698423.RATBSzdI30z_P0XCTRv4hl1G6pRB_1wQSlQzJ98Jcnrws130_assertion dcterms:description "[Since polymorphisms of TAP might influence susceptibility to Graves' disease by a possibly different selection of antigenic peptides, we investigated sequence variants of TAP1 and TAP2 genes in 235 patients with Graves' disease and 218 random healthy controls by polymerase chain reaction (PCR) followed by sequence specific oligonucleotide analysis (SSO), single strand conformational polymorphism (SSCP) analysis and amplification refractory mutation system (ARMS).]. 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:9027960 ;
    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:NP698423.RATBSzdI30z_P0XCTRv4hl1G6pRB_1wQSlQzJ98Jcnrws130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:04+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" .
}