@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP181910.RArddB_nYLMITN9HSP3CrWRxVbyD8ZgObkeyyKYUyHdcI> .
@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:NP181910.RArddB_nYLMITN9HSP3CrWRxVbyD8ZgObkeyyKYUyHdcI130_head {
  this: np:hasAssertion dgn-np:NP181910.RArddB_nYLMITN9HSP3CrWRxVbyD8ZgObkeyyKYUyHdcI130_assertion;
    np:hasProvenance dgn-np:NP181910.RArddB_nYLMITN9HSP3CrWRxVbyD8ZgObkeyyKYUyHdcI130_provenance;
    np:hasPublicationInfo dgn-np:NP181910.RArddB_nYLMITN9HSP3CrWRxVbyD8ZgObkeyyKYUyHdcI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP181910.RArddB_nYLMITN9HSP3CrWRxVbyD8ZgObkeyyKYUyHdcI130_assertion a np:Assertion .
  
  dgn-np:NP181910.RArddB_nYLMITN9HSP3CrWRxVbyD8ZgObkeyyKYUyHdcI130_provenance a np:Provenance .
  
  dgn-np:NP181910.RArddB_nYLMITN9HSP3CrWRxVbyD8ZgObkeyyKYUyHdcI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP181910.RArddB_nYLMITN9HSP3CrWRxVbyD8ZgObkeyyKYUyHdcI130_assertion {
  miriam-gene:4855 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP181910.RArddB_nYLMITN9HSP3CrWRxVbyD8ZgObkeyyKYUyHdcI130_provenance {
  dgn-np:NP181910.RArddB_nYLMITN9HSP3CrWRxVbyD8ZgObkeyyKYUyHdcI130_assertion dcterms:description
      "[We report here on the detection of nine single nucleotide polymorphisms (SNPs) near to the NOTCH4 locus in the search for schizophrenia susceptibility genes in the class III region of the human major histocompatibility complex (MHC).]. 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:14755442;
    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:NP181910.RArddB_nYLMITN9HSP3CrWRxVbyD8ZgObkeyyKYUyHdcI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:38+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;
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}