@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP282014.RAzCoBDY1-ra2PS6p0iDD4MnteroGkyyNGXAbojtsbtUk> .
@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:NP282014.RAzCoBDY1-ra2PS6p0iDD4MnteroGkyyNGXAbojtsbtUk130_head {
  this: np:hasAssertion dgn-np:NP282014.RAzCoBDY1-ra2PS6p0iDD4MnteroGkyyNGXAbojtsbtUk130_assertion ;
    np:hasProvenance dgn-np:NP282014.RAzCoBDY1-ra2PS6p0iDD4MnteroGkyyNGXAbojtsbtUk130_provenance ;
    np:hasPublicationInfo dgn-np:NP282014.RAzCoBDY1-ra2PS6p0iDD4MnteroGkyyNGXAbojtsbtUk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP282014.RAzCoBDY1-ra2PS6p0iDD4MnteroGkyyNGXAbojtsbtUk130_assertion a np:Assertion .
  dgn-np:NP282014.RAzCoBDY1-ra2PS6p0iDD4MnteroGkyyNGXAbojtsbtUk130_provenance a np:Provenance .
  dgn-np:NP282014.RAzCoBDY1-ra2PS6p0iDD4MnteroGkyyNGXAbojtsbtUk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP282014.RAzCoBDY1-ra2PS6p0iDD4MnteroGkyyNGXAbojtsbtUk130_assertion {
  miriam-gene:4698 a ncit:C16612 .
  lld:C2931822 a ncit:C7057 .
  dgn-gda:DGN1db84455a841ed88dfcedfb01d0b8f6b sio:SIO_000628 miriam-gene:4698 , lld:C2931822 ;
    a sio:SIO_001121 .
}
dgn-np:NP282014.RAzCoBDY1-ra2PS6p0iDD4MnteroGkyyNGXAbojtsbtUk130_provenance {
  dgn-np:NP282014.RAzCoBDY1-ra2PS6p0iDD4MnteroGkyyNGXAbojtsbtUk130_assertion dcterms:description "[We conclude that A1 is very rare, and A2, A11, A31, A32, A33, B8, B13, B38, B39, B44, B46, B55, B58, B61 and B71 alleles have no associations with the occurrence of NPC in Malaysia, while allele B27 is negatively associated.]. 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:17609824 ;
    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:NP282014.RAzCoBDY1-ra2PS6p0iDD4MnteroGkyyNGXAbojtsbtUk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:39+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> ;
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}