@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP419747.RAw5jEYhR6SCHtV70llYfn97XVHptF0wF4_7s61L2XF_Q> .
@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:NP419747.RAw5jEYhR6SCHtV70llYfn97XVHptF0wF4_7s61L2XF_Q130_head {
  this: np:hasAssertion dgn-np:NP419747.RAw5jEYhR6SCHtV70llYfn97XVHptF0wF4_7s61L2XF_Q130_assertion ;
    np:hasProvenance dgn-np:NP419747.RAw5jEYhR6SCHtV70llYfn97XVHptF0wF4_7s61L2XF_Q130_provenance ;
    np:hasPublicationInfo dgn-np:NP419747.RAw5jEYhR6SCHtV70llYfn97XVHptF0wF4_7s61L2XF_Q130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP419747.RAw5jEYhR6SCHtV70llYfn97XVHptF0wF4_7s61L2XF_Q130_assertion a np:Assertion .
  dgn-np:NP419747.RAw5jEYhR6SCHtV70llYfn97XVHptF0wF4_7s61L2XF_Q130_provenance a np:Provenance .
  dgn-np:NP419747.RAw5jEYhR6SCHtV70llYfn97XVHptF0wF4_7s61L2XF_Q130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP419747.RAw5jEYhR6SCHtV70llYfn97XVHptF0wF4_7s61L2XF_Q130_assertion {
  miriam-gene:57498 a ncit:C16612 .
  lld:C0011854 a ncit:C7057 .
  dgn-gda:DGN0e5abee4c95a18b8344320a36d86f211 sio:SIO_000628 miriam-gene:57498 , lld:C0011854 ;
    a sio:SIO_001121 .
}
dgn-np:NP419747.RAw5jEYhR6SCHtV70llYfn97XVHptF0wF4_7s61L2XF_Q130_provenance {
  dgn-np:NP419747.RAw5jEYhR6SCHtV70llYfn97XVHptF0wF4_7s61L2XF_Q130_assertion dcterms:description "[Since polymorphisms of TAP might influence susceptibility to IDDM possibly by selection of different antigen peptides, we investigated sequence variants of TAP1 and TAP2 genes in 120 German patients with IDDM and 218 random healthy German controls by polymerase chain reaction (PCR) followed by sequence-specific oligonucleotide analysis (SSO), single-strand conformation 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:9226129 ;
    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:NP419747.RAw5jEYhR6SCHtV70llYfn97XVHptF0wF4_7s61L2XF_Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:09+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" .
}