@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP385277.RA3Mxt-6o2Qn-4-u3iYSdUMy8L681hOZm_fxlHa2cbTPc> .
@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:NP385277.RA3Mxt-6o2Qn-4-u3iYSdUMy8L681hOZm_fxlHa2cbTPc130_head {
  this: np:hasAssertion dgn-np:NP385277.RA3Mxt-6o2Qn-4-u3iYSdUMy8L681hOZm_fxlHa2cbTPc130_assertion;
    np:hasProvenance dgn-np:NP385277.RA3Mxt-6o2Qn-4-u3iYSdUMy8L681hOZm_fxlHa2cbTPc130_provenance;
    np:hasPublicationInfo dgn-np:NP385277.RA3Mxt-6o2Qn-4-u3iYSdUMy8L681hOZm_fxlHa2cbTPc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP385277.RA3Mxt-6o2Qn-4-u3iYSdUMy8L681hOZm_fxlHa2cbTPc130_assertion a np:Assertion .
  
  dgn-np:NP385277.RA3Mxt-6o2Qn-4-u3iYSdUMy8L681hOZm_fxlHa2cbTPc130_provenance a np:Provenance .
  
  dgn-np:NP385277.RA3Mxt-6o2Qn-4-u3iYSdUMy8L681hOZm_fxlHa2cbTPc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP385277.RA3Mxt-6o2Qn-4-u3iYSdUMy8L681hOZm_fxlHa2cbTPc130_assertion {
  miriam-gene:4397 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP385277.RA3Mxt-6o2Qn-4-u3iYSdUMy8L681hOZm_fxlHa2cbTPc130_provenance {
  dgn-np:NP385277.RA3Mxt-6o2Qn-4-u3iYSdUMy8L681hOZm_fxlHa2cbTPc130_assertion dcterms:description
      "[The goal is to determine what assumptions about dependence of disease risk on genotype are consistent with data for diseases such as schizophrenia, bipolar disorder, autism, and multiple sclerosis that are relatively common (0.1-2% prevalence) and that have high concordance rates for monozygotic twins (30-50%) and high risks to first-degree relatives of affected individuals (risk ratios exceeding 4).]. 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:18689899;
    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:NP385277.RA3Mxt-6o2Qn-4-u3iYSdUMy8L681hOZm_fxlHa2cbTPc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:49+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" .
}