@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP330301.RA7vUNZYUpMABTHr2SUmQNCG9DwrVD8i2jWIpJemVRsxc> .
@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:NP330301.RA7vUNZYUpMABTHr2SUmQNCG9DwrVD8i2jWIpJemVRsxc130_head {
  this: np:hasAssertion dgn-np:NP330301.RA7vUNZYUpMABTHr2SUmQNCG9DwrVD8i2jWIpJemVRsxc130_assertion;
    np:hasProvenance dgn-np:NP330301.RA7vUNZYUpMABTHr2SUmQNCG9DwrVD8i2jWIpJemVRsxc130_provenance;
    np:hasPublicationInfo dgn-np:NP330301.RA7vUNZYUpMABTHr2SUmQNCG9DwrVD8i2jWIpJemVRsxc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP330301.RA7vUNZYUpMABTHr2SUmQNCG9DwrVD8i2jWIpJemVRsxc130_assertion a np:Assertion .
  
  dgn-np:NP330301.RA7vUNZYUpMABTHr2SUmQNCG9DwrVD8i2jWIpJemVRsxc130_provenance a np:Provenance .
  
  dgn-np:NP330301.RA7vUNZYUpMABTHr2SUmQNCG9DwrVD8i2jWIpJemVRsxc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP330301.RA7vUNZYUpMABTHr2SUmQNCG9DwrVD8i2jWIpJemVRsxc130_assertion {
  miriam-gene:1565 a ncit:C16612 .
  
  lld:C0442874 a ncit:C7057 .
  
  dgn-gda:DGNd248bdf3ecaf6abf13e65b4e5a015528 sio:SIO_000628 miriam-gene:1565, lld:C0442874;
    a sio:SIO_001121 .
}

dgn-np:NP330301.RA7vUNZYUpMABTHr2SUmQNCG9DwrVD8i2jWIpJemVRsxc130_provenance {
  dgn-np:NP330301.RA7vUNZYUpMABTHr2SUmQNCG9DwrVD8i2jWIpJemVRsxc130_assertion dcterms:description
      "[To investigate the relationship between CYP2D6 genotypes (reported to be associated with the susceptibilities to Parkinson's disease and multisystem atrophy) and the possible susceptibility to neuroleptic malignant syndrome (NMS) and subacute myelo-optico-neuropathy (SMON), we analyzed the CYP2D6 gene by polymerase chain reaction and restriction fragment length polymorphism in Japanese schizophrenia patients with a history of NMS.]. 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:9892857;
    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:NP330301.RA7vUNZYUpMABTHr2SUmQNCG9DwrVD8i2jWIpJemVRsxc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:14+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" .
}