@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP871850.RAMvQPHkLLnMKP5EtgzV7hLkpWFY3iaw608XQfaR12ESw> .
@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:NP871850.RAMvQPHkLLnMKP5EtgzV7hLkpWFY3iaw608XQfaR12ESw130_head {
   this: np:hasAssertion dgn-np:NP871850.RAMvQPHkLLnMKP5EtgzV7hLkpWFY3iaw608XQfaR12ESw130_assertion ;
    np:hasProvenance dgn-np:NP871850.RAMvQPHkLLnMKP5EtgzV7hLkpWFY3iaw608XQfaR12ESw130_provenance ;
    np:hasPublicationInfo dgn-np:NP871850.RAMvQPHkLLnMKP5EtgzV7hLkpWFY3iaw608XQfaR12ESw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP871850.RAMvQPHkLLnMKP5EtgzV7hLkpWFY3iaw608XQfaR12ESw130_assertion a np:Assertion .
  dgn-np:NP871850.RAMvQPHkLLnMKP5EtgzV7hLkpWFY3iaw608XQfaR12ESw130_provenance a np:Provenance .
  dgn-np:NP871850.RAMvQPHkLLnMKP5EtgzV7hLkpWFY3iaw608XQfaR12ESw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP871850.RAMvQPHkLLnMKP5EtgzV7hLkpWFY3iaw608XQfaR12ESw130_assertion {
   miriam-gene:10392 a ncit:C16612 .
  lld:C0023418 a ncit:C7057 .
  dgn-gda:DGNb4b6ffbf7f757862eecbcca2097a16d5 sio:SIO_000628 miriam-gene:10392 , lld:C0023418 ;
    a sio:SIO_001121 .
}
dgn-np:NP871850.RAMvQPHkLLnMKP5EtgzV7hLkpWFY3iaw608XQfaR12ESw130_provenance {
   dgn-np:NP871850.RAMvQPHkLLnMKP5EtgzV7hLkpWFY3iaw608XQfaR12ESw130_assertion dcterms:description "[NOD1/CARD4 and NOD2/CARD15 gene polymorphisms may be associated with altered risk of gastric, colorectal, breast, ovarian, prostate, testicular, lung, laryngeal, liver, gallbladder, biliary tract, pancreatic, small bowel, kidney, urinary bladder cancer, skin cancer, nonthyroid endocrine tumors, lymphoma and leukemia.]. 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:21745515 ;
    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:NP871850.RAMvQPHkLLnMKP5EtgzV7hLkpWFY3iaw608XQfaR12ESw130_publicationInfo {
   this: dcterms:created "2014-10-02T12:40:53+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" .
}