@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP340900.RAV28s0FC2fk8IBtxZHGP48OYBNO1c1J__lwv8Be9OWAM> .
@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:NP340900.RAV28s0FC2fk8IBtxZHGP48OYBNO1c1J__lwv8Be9OWAM130_head {
  this: np:hasAssertion dgn-np:NP340900.RAV28s0FC2fk8IBtxZHGP48OYBNO1c1J__lwv8Be9OWAM130_assertion;
    np:hasProvenance dgn-np:NP340900.RAV28s0FC2fk8IBtxZHGP48OYBNO1c1J__lwv8Be9OWAM130_provenance;
    np:hasPublicationInfo dgn-np:NP340900.RAV28s0FC2fk8IBtxZHGP48OYBNO1c1J__lwv8Be9OWAM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP340900.RAV28s0FC2fk8IBtxZHGP48OYBNO1c1J__lwv8Be9OWAM130_assertion a np:Assertion .
  
  dgn-np:NP340900.RAV28s0FC2fk8IBtxZHGP48OYBNO1c1J__lwv8Be9OWAM130_provenance a np:Provenance .
  
  dgn-np:NP340900.RAV28s0FC2fk8IBtxZHGP48OYBNO1c1J__lwv8Be9OWAM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP340900.RAV28s0FC2fk8IBtxZHGP48OYBNO1c1J__lwv8Be9OWAM130_assertion {
  miriam-gene:4842 a ncit:C16612 .
  
  lld:C0524528 a ncit:C7057 .
  
  dgn-gda:DGNf5b4aad5bd0520b5e1e19602a98f141d sio:SIO_000628 miriam-gene:4842, lld:C0524528;
    a sio:SIO_001121 .
}

dgn-np:NP340900.RAV28s0FC2fk8IBtxZHGP48OYBNO1c1J__lwv8Be9OWAM130_provenance {
  dgn-np:NP340900.RAV28s0FC2fk8IBtxZHGP48OYBNO1c1J__lwv8Be9OWAM130_assertion dcterms:description
      "[Diagnostic assignments of AS based on three commonly used approaches have low agreement and lead to different results in comparisons of IQ profiles, patterns of comorbidity, and familial aggregation of psychiatric symptoms across the approach-specific resultant groups of HFA, AS, and PDD-NOS.]. 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:15909408;
    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:NP340900.RAV28s0FC2fk8IBtxZHGP48OYBNO1c1J__lwv8Be9OWAM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:20+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" .
}