@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP880743.RAYFsab0jrVij6OeW5NMDTV42K8oKuS5ECkUVRm4-LtEc> .
@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:NP880743.RAYFsab0jrVij6OeW5NMDTV42K8oKuS5ECkUVRm4-LtEc130_head {
  this: np:hasAssertion dgn-np:NP880743.RAYFsab0jrVij6OeW5NMDTV42K8oKuS5ECkUVRm4-LtEc130_assertion ;
    np:hasProvenance dgn-np:NP880743.RAYFsab0jrVij6OeW5NMDTV42K8oKuS5ECkUVRm4-LtEc130_provenance ;
    np:hasPublicationInfo dgn-np:NP880743.RAYFsab0jrVij6OeW5NMDTV42K8oKuS5ECkUVRm4-LtEc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP880743.RAYFsab0jrVij6OeW5NMDTV42K8oKuS5ECkUVRm4-LtEc130_assertion a np:Assertion .
  dgn-np:NP880743.RAYFsab0jrVij6OeW5NMDTV42K8oKuS5ECkUVRm4-LtEc130_provenance a np:Provenance .
  dgn-np:NP880743.RAYFsab0jrVij6OeW5NMDTV42K8oKuS5ECkUVRm4-LtEc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP880743.RAYFsab0jrVij6OeW5NMDTV42K8oKuS5ECkUVRm4-LtEc130_assertion {
  miriam-gene:952 a ncit:C16612 .
  lld:C1848140 a ncit:C7057 .
  dgn-gda:DGN4175f2a8d52cc327b55f75ef6ae16e35 sio:SIO_000628 miriam-gene:952 , lld:C1848140 ;
    a sio:SIO_001121 .
}
dgn-np:NP880743.RAYFsab0jrVij6OeW5NMDTV42K8oKuS5ECkUVRm4-LtEc130_provenance {
  dgn-np:NP880743.RAYFsab0jrVij6OeW5NMDTV42K8oKuS5ECkUVRm4-LtEc130_assertion dcterms:description "[Animal models with genetic alterations of the OT system, like the OT, OT receptor and CD38 knock-out mice, and those with phenotypic variation in social behavior, like BTBR inbred mice and prairie voles, coupled with behavioral paradigms with face and construct validity may prove to have predictive validity for identifying the most efficacious methods of stimulating the OT system to enhance social cognition in humans.]. 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:22206823 ;
    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:NP880743.RAYFsab0jrVij6OeW5NMDTV42K8oKuS5ECkUVRm4-LtEc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:58+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> ;
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}