@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP423672.RAMfuevppCpO7JyHoCNnFXjwEoilIOlPaFKvRD0gFUvTE> .
@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:NP423672.RAMfuevppCpO7JyHoCNnFXjwEoilIOlPaFKvRD0gFUvTE130_head {
  this: np:hasAssertion dgn-np:NP423672.RAMfuevppCpO7JyHoCNnFXjwEoilIOlPaFKvRD0gFUvTE130_assertion;
    np:hasProvenance dgn-np:NP423672.RAMfuevppCpO7JyHoCNnFXjwEoilIOlPaFKvRD0gFUvTE130_provenance;
    np:hasPublicationInfo dgn-np:NP423672.RAMfuevppCpO7JyHoCNnFXjwEoilIOlPaFKvRD0gFUvTE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP423672.RAMfuevppCpO7JyHoCNnFXjwEoilIOlPaFKvRD0gFUvTE130_assertion a np:Assertion .
  
  dgn-np:NP423672.RAMfuevppCpO7JyHoCNnFXjwEoilIOlPaFKvRD0gFUvTE130_provenance a np:Provenance .
  
  dgn-np:NP423672.RAMfuevppCpO7JyHoCNnFXjwEoilIOlPaFKvRD0gFUvTE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP423672.RAMfuevppCpO7JyHoCNnFXjwEoilIOlPaFKvRD0gFUvTE130_assertion {
  miriam-gene:50488 a ncit:C16612 .
  
  lld:C2931822 a ncit:C7057 .
  
  dgn-gda:DGNd5034fade900a878b260e08bc4a5987f sio:SIO_000628 miriam-gene:50488, lld:C2931822;
    a sio:SIO_001121 .
}

dgn-np:NP423672.RAMfuevppCpO7JyHoCNnFXjwEoilIOlPaFKvRD0gFUvTE130_provenance {
  dgn-np:NP423672.RAMfuevppCpO7JyHoCNnFXjwEoilIOlPaFKvRD0gFUvTE130_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:NP423672.RAMfuevppCpO7JyHoCNnFXjwEoilIOlPaFKvRD0gFUvTE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:11+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" .
}