@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP224613.RAtVfKLCFv1AMehL4WfNj1JRWydn5IlTCIedHs7-JRpQI> .
@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:NP224613.RAtVfKLCFv1AMehL4WfNj1JRWydn5IlTCIedHs7-JRpQI130_head {
  this: np:hasAssertion dgn-np:NP224613.RAtVfKLCFv1AMehL4WfNj1JRWydn5IlTCIedHs7-JRpQI130_assertion ;
    np:hasProvenance dgn-np:NP224613.RAtVfKLCFv1AMehL4WfNj1JRWydn5IlTCIedHs7-JRpQI130_provenance ;
    np:hasPublicationInfo dgn-np:NP224613.RAtVfKLCFv1AMehL4WfNj1JRWydn5IlTCIedHs7-JRpQI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP224613.RAtVfKLCFv1AMehL4WfNj1JRWydn5IlTCIedHs7-JRpQI130_assertion a np:Assertion .
  dgn-np:NP224613.RAtVfKLCFv1AMehL4WfNj1JRWydn5IlTCIedHs7-JRpQI130_provenance a np:Provenance .
  dgn-np:NP224613.RAtVfKLCFv1AMehL4WfNj1JRWydn5IlTCIedHs7-JRpQI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP224613.RAtVfKLCFv1AMehL4WfNj1JRWydn5IlTCIedHs7-JRpQI130_assertion {
  miriam-gene:2086 a ncit:C16612 .
  lld:C1510586 a ncit:C7057 .
  dgn-gda:DGN1f189f56f1ad0bdf0c53afe9718fdbab sio:SIO_000628 miriam-gene:2086 , lld:C1510586 ;
    a sio:SIO_001121 .
}
dgn-np:NP224613.RAtVfKLCFv1AMehL4WfNj1JRWydn5IlTCIedHs7-JRpQI130_provenance {
  dgn-np:NP224613.RAtVfKLCFv1AMehL4WfNj1JRWydn5IlTCIedHs7-JRpQI130_assertion dcterms:description "[Although genetic variations in several genes encoding for synaptic adhesion proteins have been found to be associated with autism spectrum disorders, one of the most consistently replicated genes has been CNTNAP2, encoding for contactin-associated protein-like 2 (CASPR2), a multidomain transmembrane protein of the neurexin superfamily.]. 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:22872700 ;
    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:NP224613.RAtVfKLCFv1AMehL4WfNj1JRWydn5IlTCIedHs7-JRpQI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:04+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" .
}