@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP67618.RAxmxCnjxVRGJ03xlOsiluGhS75_POv5QLNm1txgIUtEo> .
@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:NP67618.RAxmxCnjxVRGJ03xlOsiluGhS75_POv5QLNm1txgIUtEo130_head {
  this: np:hasAssertion dgn-np:NP67618.RAxmxCnjxVRGJ03xlOsiluGhS75_POv5QLNm1txgIUtEo130_assertion;
    np:hasProvenance dgn-np:NP67618.RAxmxCnjxVRGJ03xlOsiluGhS75_POv5QLNm1txgIUtEo130_provenance;
    np:hasPublicationInfo dgn-np:NP67618.RAxmxCnjxVRGJ03xlOsiluGhS75_POv5QLNm1txgIUtEo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP67618.RAxmxCnjxVRGJ03xlOsiluGhS75_POv5QLNm1txgIUtEo130_assertion a np:Assertion .
  
  dgn-np:NP67618.RAxmxCnjxVRGJ03xlOsiluGhS75_POv5QLNm1txgIUtEo130_provenance a np:Provenance .
  
  dgn-np:NP67618.RAxmxCnjxVRGJ03xlOsiluGhS75_POv5QLNm1txgIUtEo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP67618.RAxmxCnjxVRGJ03xlOsiluGhS75_POv5QLNm1txgIUtEo130_assertion {
  miriam-gene:4233 a ncit:C16612 .
  
  lld:C0004352 a ncit:C7057 .
  
  dgn-gda:DGN92427b2deb1a46ac2f7efc9552505b9c sio:SIO_000628 miriam-gene:4233, lld:C0004352;
    a sio:SIO_001122 .
}

dgn-np:NP67618.RAxmxCnjxVRGJ03xlOsiluGhS75_POv5QLNm1txgIUtEo130_provenance {
  dgn-np:NP67618.RAxmxCnjxVRGJ03xlOsiluGhS75_POv5QLNm1txgIUtEo130_assertion dcterms:description
      "[To test the contribution of this functional MET promoter variant to the domains of autism, we analyzed its association with quantitative scores derived from three instruments used to diagnose and describe autism phenotypes: the Autism Diagnostic Interview-Revised (ADI-R), the Autism Diagnostic Observation Schedule (ADOS), and both the parent and the teacher report forms of the Social Responsiveness Scale (SRS).]. 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:19548256;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP67618.RAxmxCnjxVRGJ03xlOsiluGhS75_POv5QLNm1txgIUtEo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:32+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" .
}