@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP49150.RASlRvvBeVo9kO_4dBW7SqZCpB4BthzSPWKX4MhQClAHs> .
@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:NP49150.RASlRvvBeVo9kO_4dBW7SqZCpB4BthzSPWKX4MhQClAHs130_head {
  this: np:hasAssertion dgn-np:NP49150.RASlRvvBeVo9kO_4dBW7SqZCpB4BthzSPWKX4MhQClAHs130_assertion ;
    np:hasProvenance dgn-np:NP49150.RASlRvvBeVo9kO_4dBW7SqZCpB4BthzSPWKX4MhQClAHs130_provenance ;
    np:hasPublicationInfo dgn-np:NP49150.RASlRvvBeVo9kO_4dBW7SqZCpB4BthzSPWKX4MhQClAHs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP49150.RASlRvvBeVo9kO_4dBW7SqZCpB4BthzSPWKX4MhQClAHs130_assertion a np:Assertion .
  dgn-np:NP49150.RASlRvvBeVo9kO_4dBW7SqZCpB4BthzSPWKX4MhQClAHs130_provenance a np:Provenance .
  dgn-np:NP49150.RASlRvvBeVo9kO_4dBW7SqZCpB4BthzSPWKX4MhQClAHs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP49150.RASlRvvBeVo9kO_4dBW7SqZCpB4BthzSPWKX4MhQClAHs130_assertion {
  miriam-gene:150 a ncit:C16612 .
  lld:C0040517 a ncit:C7057 .
  dgn-gda:DGNfd949a4189b909ac67e158d0d7eca2eb sio:SIO_000628 miriam-gene:150 , lld:C0040517 ;
    a sio:SIO_001122 .
}
dgn-np:NP49150.RASlRvvBeVo9kO_4dBW7SqZCpB4BthzSPWKX4MhQClAHs130_provenance {
  dgn-np:NP49150.RASlRvvBeVo9kO_4dBW7SqZCpB4BthzSPWKX4MhQClAHs130_assertion dcterms:description "[These results showed that the ADRA2A gene was associated with symptoms of autonomic, sympathetic dysfunction from different diagnostic groups. The advantages of the `line item` approach include (a) the identification of the symptoms associated with each allele, (b) the identification of symptom clusters independent of DSM diagnoses, (c) the elucidation of heterosis and other mode of inheritance effects, (d) the distinction between an association with a primary disorder versus a comorbid disorder, (e) the identification of associations with sub-syndromal symptom clusters that do meet full DSM-IV criteria, and (f) the identification of symptom clusters across databases.]. 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:12627476 ;
    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:NP49150.RASlRvvBeVo9kO_4dBW7SqZCpB4BthzSPWKX4MhQClAHs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:22+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> ;
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}