@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP523655.RALokYsQ7DNrZFMm_lRSHldqfkZb52KJO2GplSWCXoTls> .
@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:NP523655.RALokYsQ7DNrZFMm_lRSHldqfkZb52KJO2GplSWCXoTls130_head {
  this: np:hasAssertion dgn-np:NP523655.RALokYsQ7DNrZFMm_lRSHldqfkZb52KJO2GplSWCXoTls130_assertion ;
    np:hasProvenance dgn-np:NP523655.RALokYsQ7DNrZFMm_lRSHldqfkZb52KJO2GplSWCXoTls130_provenance ;
    np:hasPublicationInfo dgn-np:NP523655.RALokYsQ7DNrZFMm_lRSHldqfkZb52KJO2GplSWCXoTls130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP523655.RALokYsQ7DNrZFMm_lRSHldqfkZb52KJO2GplSWCXoTls130_assertion a np:Assertion .
  dgn-np:NP523655.RALokYsQ7DNrZFMm_lRSHldqfkZb52KJO2GplSWCXoTls130_provenance a np:Provenance .
  dgn-np:NP523655.RALokYsQ7DNrZFMm_lRSHldqfkZb52KJO2GplSWCXoTls130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP523655.RALokYsQ7DNrZFMm_lRSHldqfkZb52KJO2GplSWCXoTls130_assertion {
  miriam-gene:54858 a ncit:C16612 .
  lld:C0036341 a ncit:C7057 .
  dgn-gda:DGNf08543c9052317558ae8da24a4935ef0 sio:SIO_000628 miriam-gene:54858 , lld:C0036341 ;
    a sio:SIO_001121 .
}
dgn-np:NP523655.RALokYsQ7DNrZFMm_lRSHldqfkZb52KJO2GplSWCXoTls130_provenance {
  dgn-np:NP523655.RALokYsQ7DNrZFMm_lRSHldqfkZb52KJO2GplSWCXoTls130_assertion dcterms:description "[Dysfunction of N-methyl-D-aspartate (NMDA) type ionotropic glutamate receptors has been implicated in the etiology of schizophrenia based on psychotomimetic properties of the antagonist phencyclidine (PCP) and observation that mice expressing low levels of the N-methyl-D-aspartate receptor NR1 subunit exhibit behavioral alterations that may be ameliorated by neuroleptic drugs.]. 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:11109007 ;
    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:NP523655.RALokYsQ7DNrZFMm_lRSHldqfkZb52KJO2GplSWCXoTls130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:14+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> ;
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}