@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8> .
@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:NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_head {
  this: np:hasAssertion dgn-np:NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_assertion;
    np:hasProvenance dgn-np:NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_provenance;
    np:hasPublicationInfo dgn-np:NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_assertion a np:Assertion .
  
  dgn-np:NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_provenance a np:Provenance .
  
  dgn-np:NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_assertion {
  miriam-gene:1000 a ncit:C16612 .
  
  lld:C1510586 a ncit:C7057 .
  
  dgn-gda:DGNc5b0ece49ac74b811a50009592d96b69 sio:SIO_000628 miriam-gene:1000, lld:C1510586;
    a sio:SIO_001121 .
}

dgn-np:NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_provenance {
  dgn-np:NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_assertion dcterms:description
      "[Although our data provide no overall support for association of CDH2 rare variants in these disorders considered as single entities, the clinical features and severity of probands carrying the uncommon non-synonymous variants suggest that CDH2, along with other cadherin and cell adhesion genes, is an interesting gene to pursue as a plausible contributor to OCD, TD and related disorders with repetitive behaviors, including autism spectrum disorders.]. 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:23321619;
    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:NP924749.RA1BbCpLH_EpXe7HXmW5dUPbiwFnDZDmvS9xZTFX3YUB8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:27+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" .
}