@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP797568.RAqC_Vwyy8NP0R02gTZMRSTfCTyD4b3LEsNuFA7pis-Tc> .
@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:NP797568.RAqC_Vwyy8NP0R02gTZMRSTfCTyD4b3LEsNuFA7pis-Tc130_head {
  this: np:hasAssertion dgn-np:NP797568.RAqC_Vwyy8NP0R02gTZMRSTfCTyD4b3LEsNuFA7pis-Tc130_assertion;
    np:hasProvenance dgn-np:NP797568.RAqC_Vwyy8NP0R02gTZMRSTfCTyD4b3LEsNuFA7pis-Tc130_provenance;
    np:hasPublicationInfo dgn-np:NP797568.RAqC_Vwyy8NP0R02gTZMRSTfCTyD4b3LEsNuFA7pis-Tc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP797568.RAqC_Vwyy8NP0R02gTZMRSTfCTyD4b3LEsNuFA7pis-Tc130_assertion a np:Assertion .
  
  dgn-np:NP797568.RAqC_Vwyy8NP0R02gTZMRSTfCTyD4b3LEsNuFA7pis-Tc130_provenance a np:Provenance .
  
  dgn-np:NP797568.RAqC_Vwyy8NP0R02gTZMRSTfCTyD4b3LEsNuFA7pis-Tc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP797568.RAqC_Vwyy8NP0R02gTZMRSTfCTyD4b3LEsNuFA7pis-Tc130_assertion {
  miriam-gene:4129 a ncit:C16612 .
  
  lld:C0162429 a ncit:C7057 .
  
  dgn-gda:DGNce1b310ddcc2883472051af7137c2b11 sio:SIO_000628 miriam-gene:4129, lld:C0162429;
    a sio:SIO_001121 .
}

dgn-np:NP797568.RAqC_Vwyy8NP0R02gTZMRSTfCTyD4b3LEsNuFA7pis-Tc130_provenance {
  dgn-np:NP797568.RAqC_Vwyy8NP0R02gTZMRSTfCTyD4b3LEsNuFA7pis-Tc130_assertion dcterms:description
      "[Issues that remain to be resolved are the function of the NDP gene product, the frequency and phenotype of the MAOA deficiency state, and the possible occurrence and phenotype of an MAOB deficiency state.]. 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:8541872;
    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:NP797568.RAqC_Vwyy8NP0R02gTZMRSTfCTyD4b3LEsNuFA7pis-Tc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:09+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" .
}