@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP930755.RAlU_weINf6z4n_c2fljrOqeJRIb1Qs_acJ2TTt4tq9B8> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP930755.RAlU_weINf6z4n_c2fljrOqeJRIb1Qs_acJ2TTt4tq9B8130_head {
  this: np:hasAssertion dgn-np:NP930755.RAlU_weINf6z4n_c2fljrOqeJRIb1Qs_acJ2TTt4tq9B8130_assertion;
    np:hasProvenance dgn-np:NP930755.RAlU_weINf6z4n_c2fljrOqeJRIb1Qs_acJ2TTt4tq9B8130_provenance;
    np:hasPublicationInfo dgn-np:NP930755.RAlU_weINf6z4n_c2fljrOqeJRIb1Qs_acJ2TTt4tq9B8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP930755.RAlU_weINf6z4n_c2fljrOqeJRIb1Qs_acJ2TTt4tq9B8130_assertion a np:Assertion .
  
  dgn-np:NP930755.RAlU_weINf6z4n_c2fljrOqeJRIb1Qs_acJ2TTt4tq9B8130_provenance a np:Provenance .
  
  dgn-np:NP930755.RAlU_weINf6z4n_c2fljrOqeJRIb1Qs_acJ2TTt4tq9B8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP930755.RAlU_weINf6z4n_c2fljrOqeJRIb1Qs_acJ2TTt4tq9B8130_assertion {
  miriam-gene:57502 a ncit:C16612 .
  
  lld:C3714756 a ncit:C7057 .
  
  dgn-gda:DGN8a77e6476dd55dbb6cb425928ebfe35e sio:SIO_000628 miriam-gene:57502, lld:C3714756;
    a sio:SIO_001121 .
}

dgn-np:NP930755.RAlU_weINf6z4n_c2fljrOqeJRIb1Qs_acJ2TTt4tq9B8130_provenance {
  dgn-np:NP930755.RAlU_weINf6z4n_c2fljrOqeJRIb1Qs_acJ2TTt4tq9B8130_assertion dcterms:description
      "[Mutations in neurexin 1 (NRXN1) as well as two other members of the neuroligin family, NLGN3 and NLGN4, have been associated with autism and mutations in NLGN4 have also been associated with intellectual disability, seizures, and EEG abnormalities.]. 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:22106001;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP930755.RAlU_weINf6z4n_c2fljrOqeJRIb1Qs_acJ2TTt4tq9B8130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:08+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}