@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP767253.RA7UqZradxHgHYBnamTVCUp68rnfO2zaE8N5hGpAJi8dk> .
@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:NP767253.RA7UqZradxHgHYBnamTVCUp68rnfO2zaE8N5hGpAJi8dk130_head {
  this: np:hasAssertion dgn-np:NP767253.RA7UqZradxHgHYBnamTVCUp68rnfO2zaE8N5hGpAJi8dk130_assertion ;
    np:hasProvenance dgn-np:NP767253.RA7UqZradxHgHYBnamTVCUp68rnfO2zaE8N5hGpAJi8dk130_provenance ;
    np:hasPublicationInfo dgn-np:NP767253.RA7UqZradxHgHYBnamTVCUp68rnfO2zaE8N5hGpAJi8dk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP767253.RA7UqZradxHgHYBnamTVCUp68rnfO2zaE8N5hGpAJi8dk130_assertion a np:Assertion .
  dgn-np:NP767253.RA7UqZradxHgHYBnamTVCUp68rnfO2zaE8N5hGpAJi8dk130_provenance a np:Provenance .
  dgn-np:NP767253.RA7UqZradxHgHYBnamTVCUp68rnfO2zaE8N5hGpAJi8dk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP767253.RA7UqZradxHgHYBnamTVCUp68rnfO2zaE8N5hGpAJi8dk130_assertion {
  miriam-gene:114548 a ncit:C16612 .
  lld:C0013080 a ncit:C7057 .
  dgn-gda:DGNbda9e87e8c5c66687129c8e644777e1a sio:SIO_000628 miriam-gene:114548 , lld:C0013080 ;
    a sio:SIO_001121 .
}
dgn-np:NP767253.RA7UqZradxHgHYBnamTVCUp68rnfO2zaE8N5hGpAJi8dk130_provenance {
  dgn-np:NP767253.RA7UqZradxHgHYBnamTVCUp68rnfO2zaE8N5hGpAJi8dk130_assertion dcterms:description "[Data from gene hunting in fetal DS brain along with our data on aged DS and AD patients suggest the early involvement of AVP in the pathomechanism accompanying cholinergic, monoaminergic and neuropeptidergic deficits described in DS and AD.]. 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:9739107 ;
    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:NP767253.RA7UqZradxHgHYBnamTVCUp68rnfO2zaE8N5hGpAJi8dk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:44+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" .
}