@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP377499.RAeTDm3ifyMqi1ogqudemchD9PraPKzZWkdx1Gv0bgzmg> .
@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:NP377499.RAeTDm3ifyMqi1ogqudemchD9PraPKzZWkdx1Gv0bgzmg130_head {
  this: np:hasAssertion dgn-np:NP377499.RAeTDm3ifyMqi1ogqudemchD9PraPKzZWkdx1Gv0bgzmg130_assertion ;
    np:hasProvenance dgn-np:NP377499.RAeTDm3ifyMqi1ogqudemchD9PraPKzZWkdx1Gv0bgzmg130_provenance ;
    np:hasPublicationInfo dgn-np:NP377499.RAeTDm3ifyMqi1ogqudemchD9PraPKzZWkdx1Gv0bgzmg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP377499.RAeTDm3ifyMqi1ogqudemchD9PraPKzZWkdx1Gv0bgzmg130_assertion a np:Assertion .
  dgn-np:NP377499.RAeTDm3ifyMqi1ogqudemchD9PraPKzZWkdx1Gv0bgzmg130_provenance a np:Provenance .
  dgn-np:NP377499.RAeTDm3ifyMqi1ogqudemchD9PraPKzZWkdx1Gv0bgzmg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP377499.RAeTDm3ifyMqi1ogqudemchD9PraPKzZWkdx1Gv0bgzmg130_assertion {
  miriam-gene:4842 a ncit:C16612 .
  lld:C0036341 a ncit:C7057 .
  dgn-gda:DGN3484adab58054089190b0fedd9d419b6 sio:SIO_000628 miriam-gene:4842 , lld:C0036341 ;
    a sio:SIO_001121 .
}
dgn-np:NP377499.RAeTDm3ifyMqi1ogqudemchD9PraPKzZWkdx1Gv0bgzmg130_provenance {
  dgn-np:NP377499.RAeTDm3ifyMqi1ogqudemchD9PraPKzZWkdx1Gv0bgzmg130_assertion dcterms:description "[A functional variable number of tandem repeats (VNTR) polymorphism in the promoter region of the alternative first exon 1f of NOS1 is associated with various functions of human behavior, for example increased impulsivity, while another, non-functional variant was linked to decreased verbal working memory and a heightened risk for schizophrenia.]. 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:21620982 ;
    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:NP377499.RAeTDm3ifyMqi1ogqudemchD9PraPKzZWkdx1Gv0bgzmg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:41+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" .
}