@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP184499.RANcokjSqcM77t8u8CfOOPx_QgJo5ADJRoVkwr0g0e8KI> .
@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:NP184499.RANcokjSqcM77t8u8CfOOPx_QgJo5ADJRoVkwr0g0e8KI130_head {
  this: np:hasAssertion dgn-np:NP184499.RANcokjSqcM77t8u8CfOOPx_QgJo5ADJRoVkwr0g0e8KI130_assertion ;
    np:hasProvenance dgn-np:NP184499.RANcokjSqcM77t8u8CfOOPx_QgJo5ADJRoVkwr0g0e8KI130_provenance ;
    np:hasPublicationInfo dgn-np:NP184499.RANcokjSqcM77t8u8CfOOPx_QgJo5ADJRoVkwr0g0e8KI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP184499.RANcokjSqcM77t8u8CfOOPx_QgJo5ADJRoVkwr0g0e8KI130_assertion a np:Assertion .
  dgn-np:NP184499.RANcokjSqcM77t8u8CfOOPx_QgJo5ADJRoVkwr0g0e8KI130_provenance a np:Provenance .
  dgn-np:NP184499.RANcokjSqcM77t8u8CfOOPx_QgJo5ADJRoVkwr0g0e8KI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP184499.RANcokjSqcM77t8u8CfOOPx_QgJo5ADJRoVkwr0g0e8KI130_assertion {
  miriam-gene:3126 a ncit:C16612 .
  lld:C0024305 a ncit:C7057 .
  dgn-gda:DGN3a03a7398029eddd3617af553c6a2294 sio:SIO_000628 miriam-gene:3126 , lld:C0024305 ;
    a sio:SIO_001121 .
}
dgn-np:NP184499.RANcokjSqcM77t8u8CfOOPx_QgJo5ADJRoVkwr0g0e8KI130_provenance {
  dgn-np:NP184499.RANcokjSqcM77t8u8CfOOPx_QgJo5ADJRoVkwr0g0e8KI130_assertion dcterms:description "[Finally, control participants with either HLA-DRB1*01:01 or AH 8.1 reported having a family history of NHL twice as likely as those who did not have either allele or haplotype, providing the first empirical evidence that HLA associations may explain some of the well-established relationship between family history and NHL risk.]. 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:22096508 ;
    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:NP184499.RANcokjSqcM77t8u8CfOOPx_QgJo5ADJRoVkwr0g0e8KI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:40+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" .
}