@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP169876.RAOc0Pd2CvNWqd8YkspNXjlPrr0EZa74uvq_oixFDfnCk> .
@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:NP169876.RAOc0Pd2CvNWqd8YkspNXjlPrr0EZa74uvq_oixFDfnCk130_head {
  this: np:hasAssertion dgn-np:NP169876.RAOc0Pd2CvNWqd8YkspNXjlPrr0EZa74uvq_oixFDfnCk130_assertion ;
    np:hasProvenance dgn-np:NP169876.RAOc0Pd2CvNWqd8YkspNXjlPrr0EZa74uvq_oixFDfnCk130_provenance ;
    np:hasPublicationInfo dgn-np:NP169876.RAOc0Pd2CvNWqd8YkspNXjlPrr0EZa74uvq_oixFDfnCk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP169876.RAOc0Pd2CvNWqd8YkspNXjlPrr0EZa74uvq_oixFDfnCk130_assertion a np:Assertion .
  dgn-np:NP169876.RAOc0Pd2CvNWqd8YkspNXjlPrr0EZa74uvq_oixFDfnCk130_provenance a np:Provenance .
  dgn-np:NP169876.RAOc0Pd2CvNWqd8YkspNXjlPrr0EZa74uvq_oixFDfnCk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP169876.RAOc0Pd2CvNWqd8YkspNXjlPrr0EZa74uvq_oixFDfnCk130_assertion {
  miriam-gene:3126 a ncit:C16612 .
  lld:C0011854 a ncit:C7057 .
  dgn-gda:DGN0c3d08c099b2e3d8f941fea90ea08688 sio:SIO_000628 miriam-gene:3126 , lld:C0011854 ;
    a sio:SIO_001121 .
}
dgn-np:NP169876.RAOc0Pd2CvNWqd8YkspNXjlPrr0EZa74uvq_oixFDfnCk130_provenance {
  dgn-np:NP169876.RAOc0Pd2CvNWqd8YkspNXjlPrr0EZa74uvq_oixFDfnCk130_assertion dcterms:description "[Although the difference in median birth weight was only 40 g, it may be considered significant because it appeared after segregation of the infants into two groups according to the single HLA class II allele group earlier associated with protection against, for example, childhood type 1 diabetes and certain infectious diseases.]. 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:15009177 ;
    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:NP169876.RAOc0Pd2CvNWqd8YkspNXjlPrr0EZa74uvq_oixFDfnCk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:32+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" .
}