@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP372691.RAwlntlYSfEfpbZhzCcAQWsvJTMZd2PvxCt1j5fZKvKmY> .
@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:NP372691.RAwlntlYSfEfpbZhzCcAQWsvJTMZd2PvxCt1j5fZKvKmY130_head {
  this: np:hasAssertion dgn-np:NP372691.RAwlntlYSfEfpbZhzCcAQWsvJTMZd2PvxCt1j5fZKvKmY130_assertion ;
    np:hasProvenance dgn-np:NP372691.RAwlntlYSfEfpbZhzCcAQWsvJTMZd2PvxCt1j5fZKvKmY130_provenance ;
    np:hasPublicationInfo dgn-np:NP372691.RAwlntlYSfEfpbZhzCcAQWsvJTMZd2PvxCt1j5fZKvKmY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP372691.RAwlntlYSfEfpbZhzCcAQWsvJTMZd2PvxCt1j5fZKvKmY130_assertion a np:Assertion .
  dgn-np:NP372691.RAwlntlYSfEfpbZhzCcAQWsvJTMZd2PvxCt1j5fZKvKmY130_provenance a np:Provenance .
  dgn-np:NP372691.RAwlntlYSfEfpbZhzCcAQWsvJTMZd2PvxCt1j5fZKvKmY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP372691.RAwlntlYSfEfpbZhzCcAQWsvJTMZd2PvxCt1j5fZKvKmY130_assertion {
  miriam-gene:64127 a ncit:C16612 .
  lld:C0275551 a ncit:C7057 .
  dgn-gda:DGNcce826706f35fdb4451506b0173e1a92 sio:SIO_000628 miriam-gene:64127 , lld:C0275551 ;
    a sio:SIO_001121 .
}
dgn-np:NP372691.RAwlntlYSfEfpbZhzCcAQWsvJTMZd2PvxCt1j5fZKvKmY130_provenance {
  dgn-np:NP372691.RAwlntlYSfEfpbZhzCcAQWsvJTMZd2PvxCt1j5fZKvKmY130_assertion dcterms:description "[Since they may contribute to susceptibility to spontaneous bacterial peritonitis (SBP), we studied the effects of TLR2 gene variants on susceptibility for SBP in relation to the previously reported NOD2 alleles.]. 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:21356257 ;
    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:NP372691.RAwlntlYSfEfpbZhzCcAQWsvJTMZd2PvxCt1j5fZKvKmY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:38+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" .
}