@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP113899.RAAnNZw-4023BS85H7LPiZA3k8riM6rRI_3lgiZy5FDoI> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP113899.RAAnNZw-4023BS85H7LPiZA3k8riM6rRI_3lgiZy5FDoI130_head {
  this: np:hasAssertion dgn-np:NP113899.RAAnNZw-4023BS85H7LPiZA3k8riM6rRI_3lgiZy5FDoI130_assertion;
    np:hasProvenance dgn-np:NP113899.RAAnNZw-4023BS85H7LPiZA3k8riM6rRI_3lgiZy5FDoI130_provenance;
    np:hasPublicationInfo dgn-np:NP113899.RAAnNZw-4023BS85H7LPiZA3k8riM6rRI_3lgiZy5FDoI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP113899.RAAnNZw-4023BS85H7LPiZA3k8riM6rRI_3lgiZy5FDoI130_assertion a np:Assertion .
  
  dgn-np:NP113899.RAAnNZw-4023BS85H7LPiZA3k8riM6rRI_3lgiZy5FDoI130_provenance a np:Provenance .
  
  dgn-np:NP113899.RAAnNZw-4023BS85H7LPiZA3k8riM6rRI_3lgiZy5FDoI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP113899.RAAnNZw-4023BS85H7LPiZA3k8riM6rRI_3lgiZy5FDoI130_assertion {
  miriam-gene:1312 a ncit:C16612 .
  
  lld:C0012236 a ncit:C7057 .
  
  dgn-gda:DGNf991fa4b84b9270ee29cce260c70f133 sio:SIO_000628 miriam-gene:1312, lld:C0012236;
    a sio:SIO_001122 .
}

dgn-np:NP113899.RAAnNZw-4023BS85H7LPiZA3k8riM6rRI_3lgiZy5FDoI130_provenance {
  dgn-np:NP113899.RAAnNZw-4023BS85H7LPiZA3k8riM6rRI_3lgiZy5FDoI130_assertion dcterms:description
      "[We hypothesized an interaction between the COMT(158) genotype and proline, predicting the strongest negative effect of high proline on brain function to occur in 22q11DS children who are carriers of the COMT(met) allele.]. 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:18769474;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP113899.RAAnNZw-4023BS85H7LPiZA3k8riM6rRI_3lgiZy5FDoI130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:43+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}